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:
PRODUCTION, STORAGE AND DISTRIBUTION OF: ORTHOPAD, SKIN TRACTION KIT, CANULAFIX, SURGIFIX, UMBLICAL PLASTER, ELASTOPLUS, TRI M STRIP, POLYURETHANE STRIP, EYE PATCH, SURGICAL PAD, SURGICAL SWAB, NON-WOVEN GAUZE BANDAGE, TRI M FACE MASK, NOHABIT, PEE FREE, CREP BANDAGE, TRI M UNDERPAD.
TRI M MEDICAL

Located at
605 Green land C3 Industrial zone 10th Ramadan, EL Sharikia Governorate, 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: REGULATION (EU) 2017/145 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 April 2017 This declaration of conformity is issued under the sole responsibilities of Full Support Healthcare Ltd in compliance to Article 19 of EU MDR 2017/745. Application of Council of Directive: 93/42/EEC on Medical Devices Restricted
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: 25.02.2024                                         1st Surveillance done on: 25.02.2025
Certificate Expiry:     25.02.2027                                                       2nd Surveillance: 25.02.2026

Certificate No: QACE20245