Manufacturers

Przedsiebiorstwo YAVO Sp. z o.o.

ul. Bawelniana 17 , 97-400 Belchatow
Poland

Telephone +48 44 6329411
Fax +48 44 6324917
info@yavo.com.pl

This company is co-exhibitor of
World Expo International Sp. z o.o.

Trade fair hall

  • Hall 16 / C55
 Interactive Plan

Hall map

MEDICA 2016 hall map (Hall 16): stand C55

Fairground map

MEDICA 2016 fairground map: Hall 16

Our range of products

Product categories

  • 01  Electromedical equipment / Medical Technology
  • 01.08  Surgery and Endoscopy
  • 01.08.02  Surgical instruments and products

Surgical instruments and products

  • 01  Electromedical equipment / Medical Technology
  • 01.08  Surgery and Endoscopy
  • 01.08.02  Surgical instruments and products
  • 01.08.02.08  Surgical suture materials

Surgical suture materials

Our products

Product category: Surgical instruments and products

PGA

PGA is synthetic absorbable, multifilament (braided), suture made from polyglycolic acid. Thread is coated with biocompatible polycaprolactone and calcium stearate. Thanks to its smoothness it penetrates tissues without much friction and with minimal tissue reaction. As it is a multifilament thread it is highly elastic. Atraumatic combinations of PGA are available with different types of single and double stainless steel needles. Thread can be colorless or died violet (using dyestuff C. I. Solvent Violet 13). With lapse of time, gradual loss of strength and process of absorption is visible. Absorption of PGA sutures occurs by means of hydrolysis.

Approximate % original Breaking Strength Retention:

- 80% after 14 days from implantation,
- 50% after 21 days from implantation,
- 20% after 28 days from implantation. 

Total absorption is ended after 60 - 90 days.

Atraumatic combinations of PGA are available in a range of gauge sizes and lengths, non-needled or attached to different types and sizes of single and double stainless steel needles. Violet colour is used on single and collective packaging.

PGA complies with the requirements of European Pharmacopoeia for sterile, absorbable, braided sutures.

INDICATIONS AND USE

Combination of threads PGA and needles are used according to kind and size of the wound, surgical procedures and techniques, experience of surgeon and condition of the patient. PGA are intended for use in general soft tissue, mucosa, integrating intestine and ligation other tissue including blood vessel. Use of PGA includes: general, plastic surgery, urology, orthopedic, gynecology, and obstetrics. This suture may be inappropriate in elderly, malnourished and depilated patients, or in patients suffering from conditions which may delay wound healing.

CONTRAINDICATIONS

Absorbable sutures PGA should be not used in cardiosurgery and neurosurgery. They may take place individual allergic reactions for used surgical material.

STERILITY

Sutures are sterilized by ethylene oxide gas. Do not use if package is opened or damaged. Do not resterilize. Discard opened, unused sutures. In closed packages expiry date is guaranteed till the date on the package.

STORAGE

Sutures should be storage in original packages, away from moisture and direct heat, below 25° C. Do not use after expiry date.

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Product category: Surgical instruments and products

PGA Rapid

PGA Rapid is a synthetic, absorbable, multifilament (braided) surgical thread made of hydroxyacetic acid (glycol acid). The thread is coated with biologically compliant material – polycaprolactone and calcium stearate. Precise, uniform structure gives the thread an even surface with relatively low friction and strong tightening of knots as well as minimum reaction of tissues.

Special strength of the multifilament structure enables high tensility.

The thread is available in natural colour (beige). With the time, the resistance to stretch is lowering and the final absorption as a result of hydrolysis. % of the original Breaking Strength Retention:

- about 65% after 7 days from implementation,
- about 50 % after 8-11 days from implementation.

The absorption is complete after 42.

Atraumatic combinations of the threads are manufactured in different lengths and sizes and are furnished with single or double stainless steel needles of different type and size. The product is also available without the needle as a ligature. The unit package and the label are light red.

All the combinations and the threads themselves meet the requirements of the European Pharmacopoeia for sterile, absorbable, single-fibre surgical thread.

INDICATIONS AND USAGE

The PGA rapid surgical thread is recommended when only a short-term joining of the wound edges is required and quick absorption of the thread is advantageous. Combinations of PGA Rapid threads and needles depend on the type and size of a patient’s wounds, the area, the surgical techniques, the surgeon’s experience and the patient’s condition. The threads are mainly recommended for soft tissues and closing the dermal wounds, especially in pediatric surgery. The PGA Rapid thread is also used for closing the wounds of the mouth mucous membrane and in the eye surgery. Surgical use of the thread includes: general and plastic surgery, ophthalmology and gynecology.

CONTRADICTIONS

Due to its short-term wound support and absorption, the PGA Surgical thread should not be used in places when longer support of wound edges is required. No contradictions for use in cardiac surgery and neurosurgery. The tread is not applied for tying off. Individual allergic reactions to the suture material may occur.

STERILITY INDICATIONS

The suture is sterilised with ethylene oxide. If the package is broken, the suture may not be used. The content of the package should not be sterilised again. Unused thread, after the sterile bag is open, may not be used later. In closed packages, sterility is guaranteed by the expiry date.

STORAGE CONDITIONS

The sutures should be stored in original package, in dry and airy places, free from humidity and direct sunlight, in the temperature lower than 25 °C. Do not use after the expiry date.

SYMBOLS USED ON LABELS

Disposable
Expiry date
Read the Manual
Sterilised with ethylene oxide
Catalogue number

The CE mark and the ID of the notified organisation. The product meets the basic requirements of the 93/42/EWG Directive – Medical Devices and the Amending Directive 2007/47

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Product category: Surgical instruments and products

PGLA Lactic

PGLA LACTIC is a synthetic, absorbable, braided surgical thread, made of a poly(glycolide-co-L-lactide) (90/10). The thread is coated with a mixture of poly(glycolide-co-L-lactide) (30/70) and calcium stearate. The coating increases smoothness of the thread surface enabling precise tying of the suture and a tight and sure knot. It also reduces tissue traumatisation.

The PGLA LACTIC thread may be natural (beige) or purple (coloured with C. I. Solvent Violet 13 colorant). With the time, the resistance to stretch is lowering and the final absorption as a result of hydrolysis takes place. % of the original Breaking Strength Retention:

- 75% after 14 days from implantation,
- 50 % after 21 days from implantation,
- 25 % after 28 days from implantation.

The absorption is complete after – 60-70 days from implantation.

Atraumatic combinations of the threads are manufactured in different lengths and sizes and are furnished with single or double stainless steel needles of different type and size. The product is also available without the needle as a ligature. The unit package and the label are beige. The PGLA LACTIC surgical threads meet the requirements of the Polish and European Pharmacopoeia.

INDICATIONS AND USE
Combinations of PGLA LACTIC threads and needles depend on the type and size of a patient’s wounds, the area, the surgical techniques, the surgeon’s experience and the patient’s condition. The threads are mainly recommended for soft tissues (subcutaneous tissues, mucous membrane) and/or tying off tissues, which do not require prolonged action of the ligature). Surgical use of the thread includes: general, paediatric and plastic surgery, urology, orthopaedics, gynaecology and obstetrics. They are also used in dental surgery and for joining mucous membrane in mouth, as well as eye surgery, for joining peripheral nerves and blood vessels.

CONTRAINDICATIONSThe absorbable PGLA LACTIC thread should not be applied, when prolonged joining of tissues is necessary. The suture may cause gentle tissue reaction during absorption. Any significant contradictions for PGLA LACTIC have been described. Basically not used in cardiac and vascular surgery. When using PGLA LACTIC sutures, worse absorption in case of older, malnourished and weakened people as well as patients in a condition, which might extend the process of tissue healing should be taken into account. Individual allergic responses to the suture may occur.

STERILITY

If the package is broken, the suture may not be used. The package content should not be sterilised again. In closed and not impaired packages, sterility is guaranteed by the expiry date.  The PGLA LACTIC suture is a disposable material for one patient only. Unused thread, after the sterile bag is open, may not be used later. Do not reuse as the suture is not sterile or non-pyrogenic anymore and may be biologically infected.

STORAGEThe sutures should be stored in an original package, in dry and airy places, free from humidity and direct sunlight, at the temperature below 25 °C.  Do not use after expiry date.

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Product category: Surgical instruments and products

Monofast

MONOFAST is monofilament, synthetic absorbable suture. It consists of glycolic acid and caprolactone polymer. Thread can be died violet (using dyestuff C. I. Solvent Violet 13). Monofast easily penetrates tissues, has high initial tensile strength. With lapse of time, gradual loss of strength and process of absorption is visible. Absorption of Monofast sutures occurs by means of hydrolysis.

Approximate % original Breaking Strength Retention:

- 70% after 7 days from implantation,
- 40% after 14 days from implantation,
- 15% after 21 days from implantation,
- 5% after 28 days from implantation. 

Total absorption is ended after 90 – 120 days.

Atraumatic combinations of MONOFAST are available in a range of gauge sizes and lengths, non-needled or attached to different types and sizes of single and double stainless steel needles. Light orange colour is used on single and collective packaging.

INDICATIONS AND USE

Combination of threads Monofast and needles are used according to kind and size of the wound, surgical procedures and techniques, experience of surgeon and condition of the patient. Monofast are intended for use in general soft tissue and/or they ligation in case absorbable sutures are needed. Use of Monofast includes: general, child, plastic surgery, urology, orthopedic, gynecology, and gastrology. This suture may be inappropriate in cardiovascular, neural tissue, microsurgery and ophthalmic surgery.

CONTRAINDICATIONS

Absorbable sutures Monofast should be not used where extended approximation of tissues under stress is required, alternatively the use of supplemental non-absorbable sutures should be considered by the surgeon by using Monofast in that case. They may take place individual allergic reactions for used surgical material. Use of Monofast in urinary and biliary tracts surgery may result in calculs formation.

STERILITY

Sutures are sterilized by ethylene oxide gas. Do not use if package is opened or damaged. Do not resterilize. Discard opened, unused sutures. In closed packages expiry date is guaranteed till the date on the package.

STORAGE

Sutures should be storage in original packages, away from moisture and direct heat, below 25° C. Do not use after expiry date.

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Product category: Surgical instruments and products

Monosorb

MONOSORB is monofilament, synthetic absorbable suture, made from polydioxanone. Thread can be colorless (beige) or died violet (using dyestuff C. I. Solvent Violet 13). Monosorb easily penetrates tissues, has high initial tensile strength. With lapse of time, gradual loss of strength and process of absorption is visible. Absorption of Monosorb sutures occurs by means of hydrolysis.

Approximate % original Breaking Strength Retention:

1. For thread sizes 4/0 and smaller:

- 75% after 14 days from implantation,
- 65% after 28 days from implantation,
- 55% after 43 days from implantation, 
- 40% after 57 days from implantation. 

2. For thread sizes 3/0 and bigger:

- 75% after 14 days from implantation,
- 70% after 28 days from implantation,
- 60% after 43 days from implantation,
- 40% after 57 days from implantation. 

Total absorption is ended after 90 – 120 days.

Atraumatic combinations of MONOSORB are available in a range of gauge sizes and lengths, non-needled or attached to different types and sizes of single and double stainless steel needles. Blue colour is used on single and collective packaging.

MONOSORB complies with the requirements of European Pharmacopoeia for sterile, absorbable, monofilament sutures.

INDICATIONS AND USE

Combination of threads Monosorb and needles are used according to kind and size of the wound, surgical procedures and techniques, experience of surgeon and condition of the patient. Monosorb is intended for use in where long term wound support is required. Monosorb is intendet to use in pediatric cardiovascular and ophthalmic surgery. Use of Monosorb includes: general, plastic surgery, urology, orthopedic and gynecology. This suture may be inappropriate in elderly, malnourished or debilitated patients, or in patients suffering from conditions which may delay wound healing.

CONTRAINDICATIONS

Adverse reactions associated with this device included: transient local irritation at the wound site, transient inflammatory foreign body response.

Absorbable sutures Monosorb should be not used where extended approximation of tissues under stress is required, alternatively the use of supplemental non-absorbable sutures should be considered by the surgeon by using Monosorb in that case. They may take place individual allergic reactions for used surgical material. Monosorb should be not use in adult cardiovascular surgery, microsurgery.

STERILITY

Sutures are sterilized by ethylene oxide gas. Do not use if package is opened or damaged. Do not resterilize. Discard opened, unused sutures. In closed packages expiry date is guaranteed till the date on the package.

STORAGE

Sutures should be storage in original packages, away from moisture and direct heat, below 25° C. Do not use after expiry date.

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About us

Company details

YAVO Sp. z o.o. is a Polish manufacturer of medical supplies. For years, we have gathered experience and knowledge, which make us able to offer the highest quality medical supplies. Every day, the dynamics of the medical supplies market brings us new challenges, we are able to handle with our qualified personnel. Our offer of surgical sutures is constantly growing, so we can compete with the products of international corporations, while keeping the prices low.

The advantages of YAVO sutures have been known to our customers from Germany, France, Hungary, Romania and Cyprus - they appreciate both the quality and the dynamics, short deadlines and reliability, confirmed with the ISO 13485 Quality Management System for Medical. Products and the CE Certificates.

   A Polish product-it is a responsibility!

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