IMPORTANT NOTE:
These technical specifications are generic and may vary depending on the selected Vendor.
Product description:
Plastic jar for containing forceps, smooth surface without cover
Material: Polypropylene
Autoclavable at 121 °C
Without cover.
Internal diameter: approx. 54mm.
Depth: approx. 180 mm.
Overall height: approx. 200mm.
Instructions for use:
Used to hold sterile serving forceps;
This item must be cleaned, disinfected and sterilized in a steam steriliser as often as necessary.
Supplied with:
Manufacturer's instruction for use.
Packaging and labelling:
Unit presentation: plastic film, non-sterile.
Labelling on the primary packaging:
Name and/or trademark and address of the manufacturer..
Manufacturer's product reference
Symbols used according ISO 15223 and EN 980
CE mark
Regulation & conformity requirements:
CE mark conforming to Medical Device Directive 93/42/EEC
CE self-declaration.
ISO 13485:2003 certified
Classification:
Class I-Medical Device Directive 93/42/EEC
Safety & product Standards:
ISO 13485: 2003 Quality management systems -- Requirements for regulatory purposes
ISO 14971:2007 Medical Devices- Application of risk management to medical devices
ISO 17664:2004 Sterilization of medical devices -- Information to be provided by the manufacturer for the processing of re-sterilizable medical devices
Environmental requirements:
Not use PVC polymer
These technical specifications are generic and may vary depending on the selected Vendor.
Product description:
Plastic jar for containing forceps, smooth surface without cover
Material: Polypropylene
Autoclavable at 121 °C
Without cover.
Internal diameter: approx. 54mm.
Depth: approx. 180 mm.
Overall height: approx. 200mm.
Instructions for use:
Used to hold sterile serving forceps;
This item must be cleaned, disinfected and sterilized in a steam steriliser as often as necessary.
Supplied with:
Manufacturer's instruction for use.
Packaging and labelling:
Unit presentation: plastic film, non-sterile.
Labelling on the primary packaging:
Name and/or trademark and address of the manufacturer..
Manufacturer's product reference
Symbols used according ISO 15223 and EN 980
CE mark
Regulation & conformity requirements:
CE mark conforming to Medical Device Directive 93/42/EEC
CE self-declaration.
ISO 13485:2003 certified
Classification:
Class I-Medical Device Directive 93/42/EEC
Safety & product Standards:
ISO 13485: 2003 Quality management systems -- Requirements for regulatory purposes
ISO 14971:2007 Medical Devices- Application of risk management to medical devices
ISO 17664:2004 Sterilization of medical devices -- Information to be provided by the manufacturer for the processing of re-sterilizable medical devices
Environmental requirements:
Not use PVC polymer
| Pack Size | Avg. Price |
|---|---|
| Pack of 1 | $6.18 |
