IMPORTANT NOTE:
These technical specifications are generic and may vary depending on the selected Vendor.
Intended purpose of use: commonly used to hold and transport medical consumables of instruments for a procedure
Product description:
Kidney shaped container made of polypropylene used for general ward use.
Material: Polypropylene, autoclavable
Length: approx. 205mm
Width: approx. 95mm
Height: approx. 45mm
Capacity: approx. 475ml (±5% tolerance limit)
Reusable, Autoclavable 121 Deg C
Shall be supplied with cleaning, disinfecting and sterilization instructions.
Shall provide the approximate weight of the item (±5% tolerance limit)
Packaging and labelling:
Over packaging: Packaging unit
Labelling on the packaging unit:
Name and address of the manufacturer. Provide brand name/trade mark details if any.
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""(of equivalent harmonised symbol), if applicable.
Information for particular storage conditions (temperature, pressure, light, humidity, etc.), as appropriate (of equivalent harmonised symbol).
Information for handling, if applicable (of equivalent harmonised symbol).
Symbols used according ISO 15223
CE Mark
Instructions for use:
to be provided in English/French/Arabic/Spanish.
Basic equipment for nursing and surgical use.
cleaning, disinfecting and sterilization instructions, list of non computable disinfectants, if any.
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 (as per latest revisions of the product standards):
ISO 7153-1:1991 Surgical instruments --Metallic materials --Part 1: Stainless steel
These technical specifications are generic and may vary depending on the selected Vendor.
Intended purpose of use: commonly used to hold and transport medical consumables of instruments for a procedure
Product description:
Kidney shaped container made of polypropylene used for general ward use.
Material: Polypropylene, autoclavable
Length: approx. 205mm
Width: approx. 95mm
Height: approx. 45mm
Capacity: approx. 475ml (±5% tolerance limit)
Reusable, Autoclavable 121 Deg C
Shall be supplied with cleaning, disinfecting and sterilization instructions.
Shall provide the approximate weight of the item (±5% tolerance limit)
Packaging and labelling:
Over packaging: Packaging unit
Labelling on the packaging unit:
Name and address of the manufacturer. Provide brand name/trade mark details if any.
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""(of equivalent harmonised symbol), if applicable.
Information for particular storage conditions (temperature, pressure, light, humidity, etc.), as appropriate (of equivalent harmonised symbol).
Information for handling, if applicable (of equivalent harmonised symbol).
Symbols used according ISO 15223
CE Mark
Instructions for use:
to be provided in English/French/Arabic/Spanish.
Basic equipment for nursing and surgical use.
cleaning, disinfecting and sterilization instructions, list of non computable disinfectants, if any.
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 (as per latest revisions of the product standards):
ISO 7153-1:1991 Surgical instruments --Metallic materials --Part 1: Stainless steel
| Pack Size | Avg. Price |
|---|---|
| Pack of 1 | $1.32 |
