IMPORTANT NOTE:
These technical specifications are generic and may vary depending on the selected Vendor.
Product description:
Abdominal retractor with locking mechanism (self-holding).
Three (3) blades, the two side blades being mobile and the middle blade removable.
Used to retract the abdominal wall and viscera to provide good exposure of the operative field.
Material: Martensitic steel (quenched, magnetic steel).
Composition: From 0.42% to 0.55% carbon; From 12% to 15% chromium; From 0.45% to 0.9% molybdenum.
Solid lateral blades: approx. 38 x 60 mm.
Solid center blade: approx. 38 x 55 mm.
Maximum wound opening: approx. 100 mm.
Solid center blade: approx. 45 x 80 mm.
Maximum wound opening: approx. 180 mm.
Supplied with:
Manufacturer's instruction for use.
Instructions for use:
To retract skin, fatty tissue, muscles or viscera after the incision to expose the operative field.
This item must be cleaned, disinfected after each use, and sterilised in a steam steriliser.
CE mark
Packaging & Labelling:
Primary packaging: Unit of use
One (1) retractor in a plastic bag.
Labelling on the primary packaging:
Name and/or trademark of the manufacturer.
Manufacturer's product reference.
Type of product and main characteristics.
If the packaging is not transparent, it must bear a diagram (preferably actual size) showing the essential parts of the product and indicating the position of the product in the packaging.
Lot number prefixed by the word "LOT"(or equivalent harmonised symbol), if applicable.
Information for particular storage conditions (temperature, pressure, light, humidity, etc.), as appropriate or equivalent harmonised symbol.
Information for handling, if applicable (or equivalent harmonised symbol).
Symbols used according ISO 15223
Over packaging: Packaging unit.
CE mark
Regulation & conformity requirements:
CE mark conforming to Medical Device Directive 93/42/EEC
CE self-declaration.
ISO 13845:2003 certified
Classification:
Class I (MDD 93/42/EEC)
Safety & product Standards:
Must comply with following standards
ISO 7153-1:1991 Surgical instruments -- Metallic materials -- Part 1: Stainless steel
ISO 7151:1988 Surgical instruments -- Non-cutting, articulated instruments -- General requirements and test methods
ISO 17664:2004 Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices
These technical specifications are generic and may vary depending on the selected Vendor.
Product description:
Abdominal retractor with locking mechanism (self-holding).
Three (3) blades, the two side blades being mobile and the middle blade removable.
Used to retract the abdominal wall and viscera to provide good exposure of the operative field.
Material: Martensitic steel (quenched, magnetic steel).
Composition: From 0.42% to 0.55% carbon; From 12% to 15% chromium; From 0.45% to 0.9% molybdenum.
Solid lateral blades: approx. 38 x 60 mm.
Solid center blade: approx. 38 x 55 mm.
Maximum wound opening: approx. 100 mm.
Solid center blade: approx. 45 x 80 mm.
Maximum wound opening: approx. 180 mm.
Supplied with:
Manufacturer's instruction for use.
Instructions for use:
To retract skin, fatty tissue, muscles or viscera after the incision to expose the operative field.
This item must be cleaned, disinfected after each use, and sterilised in a steam steriliser.
CE mark
Packaging & Labelling:
Primary packaging: Unit of use
One (1) retractor in a plastic bag.
Labelling on the primary packaging:
Name and/or trademark of the manufacturer.
Manufacturer's product reference.
Type of product and main characteristics.
If the packaging is not transparent, it must bear a diagram (preferably actual size) showing the essential parts of the product and indicating the position of the product in the packaging.
Lot number prefixed by the word "LOT"(or equivalent harmonised symbol), if applicable.
Information for particular storage conditions (temperature, pressure, light, humidity, etc.), as appropriate or equivalent harmonised symbol.
Information for handling, if applicable (or equivalent harmonised symbol).
Symbols used according ISO 15223
Over packaging: Packaging unit.
CE mark
Regulation & conformity requirements:
CE mark conforming to Medical Device Directive 93/42/EEC
CE self-declaration.
ISO 13845:2003 certified
Classification:
Class I (MDD 93/42/EEC)
Safety & product Standards:
Must comply with following standards
ISO 7153-1:1991 Surgical instruments -- Metallic materials -- Part 1: Stainless steel
ISO 7151:1988 Surgical instruments -- Non-cutting, articulated instruments -- General requirements and test methods
ISO 17664:2004 Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices
| Pack Size | Avg. Price |
|---|---|
| Pack of 1 | $47.07 |
