Intended purpose of use: Rochester-Pean haemostatic forceps are used for clamping larger tissue and vessels for haemostasis.
Product description: Haemostatic forceps, Rochester-Pean, curved for haemostasis, gripping, dissection and tampon holder. The full horizontal serrations and availability in multiple lengths make these forceps a versatile instrument used in multiple procedures.
Curved.
Material: Martensitic stainless steel (quenched, magnetic steel) composition: 0.20% carbon; 13% chromium.
Springy.
locking.
Variable setting of ratchet, lockable.
Non traumatic jaws with full horizontal jaw serrations.
Adjustment of jaws.
Without teeth.
Highly impact resistant.
Length: approx.160 mm.
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:
Used for haemostasis, gripping, dissection and tampon holder.
This item must be cleaned, disinfected after each use, and sterilised in a steam steriliser.
Packaging & Labelling:
One (1) forceps 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.
SO 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, Rochester-Pean, curved for haemostasis, gripping, dissection and tampon holder. The full horizontal serrations and availability in multiple lengths make these forceps a versatile instrument used in multiple procedures.
Curved.
Material: Martensitic stainless steel (quenched, magnetic steel) composition: 0.20% carbon; 13% chromium.
Springy.
locking.
Variable setting of ratchet, lockable.
Non traumatic jaws with full horizontal jaw serrations.
Adjustment of jaws.
Without teeth.
Highly impact resistant.
Length: approx.160 mm.
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:
Used for haemostasis, gripping, dissection and tampon holder.
This item must be cleaned, disinfected after each use, and sterilised in a steam steriliser.
Packaging & Labelling:
One (1) forceps 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.
SO 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 | $2.29 |
