Application of Council of Directive: 93/42/EEC on Medical Devices Restricted To the Aspects of Manufacture Concerned with Securing and
Maintaining Sterile Conditions.
This Is to Certify That Technical Documentation for The Products:
PRODUCT DESCRIPTION: (GAUZE, MEDICAL COTTON, COTTON LIGAMENT, DRESSING SWAP, BED COVER, ELASTIC BANDAGE, PARAFFIN GAUZE, OXYGEN MASKS, NEBULIZER MASK, COLON MEDICAL SUPPLIES, DOCTOR GOWNS, FACE MASK AND NON-WOVEN FABRICS, BED SHEETS, OVERHEAD, SHOES COVER, COVERALL, CUSHION (FOR HAEMORRHOIDS), WET WIPED WITH ALCOHOL/ACETONE. IV SET, CUPPING CUP, RUBBER HOT WATER BOTTLE, STERILIZATION ROLL PAPER, STERILIZATION POUCHES, ORTHOPEDIC PADDING BANDAGE) STERILE AND NON-STERILE.

CARE PLUS FOR HEALTH CARE PRODUCTS
Located at
12 EL BANNA ST., INDUSTRIAL ZONE, MAHALA EL KOBRA – EGYPT.

has been assessed and found in accordance with the Requirements of:
The Technical document maintained by the organization has been reviewed and found to comply with the requirements of Directive: 93/42/EEC on Medical Devices
This certificate of compliance is based on the technical file of above-mentioned product, Technical Reports and documentation are at the organization’s, this is to certify that the product is in conformity with all revision of Council Directive 93/42/EEC referred to medical devices, this certificate does not imply assessment of series production of product and does not permit use of Euro Compliance
QAS international. Mark of conformity, Further Identification and description of products covered by this certificate

Certificate Issuance: 23.01. 2023                                   1st Surveillance done on: 23.01. 2024
Certificate Expiry:     23.01. 2026                                  2nd Surveillance done on: 23.01. 2025

Certificate No: QACE20220109