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:
PRODUCTS DESCRIPTION:
PRODUCTION, STORAGE AND DISTRIBUTION OF MEDICALCOTTON.
TABI MANUFACTORY
Located at
Al Othmaneyah, El Mahalla El Kubra, Gharbia, Egypt.
has been assessed and found in accordance with the Requirements of:
We hereby certify that the under mentioned manufacturer has established and maintains a full
quality assurance system according to the requirements of Directive 93/42/EEC, annex II (with the
exemption of section 4) For the design, manufacturing and final inspection of the products mentioned
in the certificate.
Any significant changes in the design or manufacturing may render this certificate invalid.
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: 10.11. 2025
1st Surveillance: 10.11.2026
2nd Surveillance: 10.11.2027
Certificate Expiry: 10.11. 2028

---

Certificate No: QACE20240795