Intended purpose of use: Curved scissor is most commonly utilized for cutting of dissecting dense of deep tissue and the straight version is typically used for cutting surface tissue of sutures. Both may be used interchangeably depending on procedure and physician preference.
Product description: Surgical dissecting scissors, Mayo.
Material: Martensitic stainless steel (quenched, magnetic steel) composition: 0.40 % carbon; 14% chromium.
Instrument that cuts by shearing.
Thin, curved, with blunt end blades.
Length: approx. 230mm.
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:
Surgical dissecting scissors used for non-delicate dissections and to cut sutures and dressings.
This item must be cleaned, disinfected after each use, and sterilised in a steam steriliser.
Packaging & Labelling:
Unit presentation: individually, in protective packaging.
The following should appear on the packaging:
- Designation of the instrument.
- Name and address of supplier (manufacturer).
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 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.
ISO 7741 Instruments for surgery -- Scissors and shears -- General requirements and test methods.
Environmental requirements: ISO 14001.
Product description: Surgical dissecting scissors, Mayo.
Material: Martensitic stainless steel (quenched, magnetic steel) composition: 0.40 % carbon; 14% chromium.
Instrument that cuts by shearing.
Thin, curved, with blunt end blades.
Length: approx. 230mm.
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:
Surgical dissecting scissors used for non-delicate dissections and to cut sutures and dressings.
This item must be cleaned, disinfected after each use, and sterilised in a steam steriliser.
Packaging & Labelling:
Unit presentation: individually, in protective packaging.
The following should appear on the packaging:
- Designation of the instrument.
- Name and address of supplier (manufacturer).
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 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.
ISO 7741 Instruments for surgery -- Scissors and shears -- General requirements and test methods.
Environmental requirements: ISO 14001.
| Pack Size | Avg. Price |
|---|---|
| Pack of 1 | $3.70 |
