Intended purpose of use: to provide an atraumatic way to clamp blood vessels, hold needles and grasp tissues. Used for haemostasis in deep surgery
Product description: Haemostatic forceps, Crafoord, also be known as a Crafoord Coarctation Clamp, may also be identified by the name Coller. Not intended for nursing care.
Material: Martensitic stainless steel (quenched, magnetic steel) composition: 0.20% carbon; 13% chromium.
Spring-type
slightly curved jaws with inner serrations
Flexible arms with finger ring handle
Progressive setting of the ratchet.
Variable settings of the ratchet, lockable.
Highly impact resistant.
Length: approx. 240mm.
Supplied non sterile, Hygienically packed for medical use after sterilization.
Reusable: Can withstand repeated reprocessing including steam sterilization, including manual brushing and the use of disinfectant chemicals
Supplied with:
Manufacturer's instruction for use
Instructions for use:
Haemostatic forceps, Crawford, used for deep haemostasis, not intended for nursing care This item must be cleaned, disinfected after each use, and sterilised in a steam steriliser.
Packaging & Labelling:
Unit presentation: forceps single unit, in a plastic bag.
Symbols used according ISO 15223
CE mark, Labelling as per regulations applied to the device. Shall include name of the device, name and address of the manufacturer, product code of manufacturers reference number etc.
Regulatory & Conformity Requirements:
CE mark Comply to EU Council Directive 93/42/EEC (MDD) of EU Regulations 2017/745 (MDR) with valid EC Certificate and Declaration of Conformity for the CE mark is applicable.
US FDA 510(K) clearance
CE certificate available for Class IIa and above devices
Manufacturer’s Quality Management System is certified to ISO 13485 : 2016
Classification:
Classified under EU MDR 2017/745 as Class I device
Safety & product Standards:
Must comply with the following standards (as per latest revision of standards):
ISO 14971:2007 Medical Devices- Application of risk management to medical devices
ISO 7153-1:1991/Amd1:1999 Surgical instruments- Metallic material – Part 1 Stainless Steel
ISO 7151:1988 Surgical instruments -- Non-cutting, articulated instruments -- General requirements and test methods
ISO 13402:1995 Surgical and dental hand instruments -- Determination of resistance against autoclaving, corrosion and thermal exposure
ISO 17664:2004 Sterilization of medical devices -- Information to be provided by the manufacturer for the processing of re-sterilizable medical devices
Environmental requirements:
ISO 14001
Product description: Haemostatic forceps, Crafoord, also be known as a Crafoord Coarctation Clamp, may also be identified by the name Coller. Not intended for nursing care.
Material: Martensitic stainless steel (quenched, magnetic steel) composition: 0.20% carbon; 13% chromium.
Spring-type
slightly curved jaws with inner serrations
Flexible arms with finger ring handle
Progressive setting of the ratchet.
Variable settings of the ratchet, lockable.
Highly impact resistant.
Length: approx. 240mm.
Supplied non sterile, Hygienically packed for medical use after sterilization.
Reusable: Can withstand repeated reprocessing including steam sterilization, including manual brushing and the use of disinfectant chemicals
Supplied with:
Manufacturer's instruction for use
Instructions for use:
Haemostatic forceps, Crawford, used for deep haemostasis, not intended for nursing care This item must be cleaned, disinfected after each use, and sterilised in a steam steriliser.
Packaging & Labelling:
Unit presentation: forceps single unit, in a plastic bag.
Symbols used according ISO 15223
CE mark, Labelling as per regulations applied to the device. Shall include name of the device, name and address of the manufacturer, product code of manufacturers reference number etc.
Regulatory & Conformity Requirements:
CE mark Comply to EU Council Directive 93/42/EEC (MDD) of EU Regulations 2017/745 (MDR) with valid EC Certificate and Declaration of Conformity for the CE mark is applicable.
US FDA 510(K) clearance
CE certificate available for Class IIa and above devices
Manufacturer’s Quality Management System is certified to ISO 13485 : 2016
Classification:
Classified under EU MDR 2017/745 as Class I device
Safety & product Standards:
Must comply with the following standards (as per latest revision of standards):
ISO 14971:2007 Medical Devices- Application of risk management to medical devices
ISO 7153-1:1991/Amd1:1999 Surgical instruments- Metallic material – Part 1 Stainless Steel
ISO 7151:1988 Surgical instruments -- Non-cutting, articulated instruments -- General requirements and test methods
ISO 13402:1995 Surgical and dental hand instruments -- Determination of resistance against autoclaving, corrosion and thermal exposure
ISO 17664:2004 Sterilization of medical devices -- Information to be provided by the manufacturer for the processing of re-sterilizable medical devices
Environmental requirements:
ISO 14001
| Pack Size | Avg. Price |
|---|---|
| Pack of 1 | $3.96 |
