Holma Inc Ce

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Certificate of Compliance

We hereby declare that the technical file of product complied with the requirements of Medical Device Directive
93/42/EEC & EU Council Directive: 2004/108/EC & 2006/95/EC as Amended
Certificate Number: CE- 202104362234GS
Manufacturer
Name : HOLMA INC.
Address : MEZZANINE FLOOR, M 5, SATYAWATI COLONY, ASHOK VIHAR PHASE-3, DELHI,
NORTH WEST DELHI, DELHI-110052 INDIA.
Products : Medical instruments and Equipments, Surgical instruments and Equipments, Scientific
instruments and Equipments, Nitrile gloves, Latex gloves, Vinyl gloves, 2/3/4 Ply masks, N95 masks, KN95 masks, Surgical
masks, FFP 1/2/3 masks, Surgical gowns, Shoe covers, Head covers, PPE kits, Hand Sanitizer, Alcohol Wipes, Oximeters,
Infrared Thermometers, Digital Thermometers, Syringes, Sodium Citrate Tubes, Swabs, Medical Kits, All types of
Chemicals, Oils, Fresh Vegetables, Fresh Fruits, Tea, Incense Sticks, Stationary Items, Educationals Kits, Corrugated Boxes,
Kraft Paper, Household Items, Handicrafts, Furniture, Crockery, Scrap.

The Certification body has performed an audit of the above product quality system covering the design, manufacture and final inspection of the
certified product. The quality system has been assessed, approved and is subject to continuous surveillance according to the directive Medical
Device Directive 93/42/EEC & EU Council Directive: 2004/108/EC & 2006/95/EC as Amended.

This certificate is issued under the following conditions:

1. It applies only to the quality system maintained in the manufacture of above referenced models and it does not substitute the
design or type-examination procedures, if requested.
2. The certificate remains valid until the manufacturing conditions or the quality systems are changed.
3. The certificate validity is conditioned by positive results or surveillance audits.
The CE mark as shown above can be used, under the responsibility of the manufacturer, after completion of an EC Declaration of
conformity and compliance with all relevant EC Directives. The statement is based on a single evaluation of one sample of abo ve mentioned
product. It does not imply an assessment of the whole production.

Date of Certification: 07th June 2021 2nd Surveillance Audit Due: 06th June 2023
1st Surveillance Audit Due: 06th June 2022 Certificate Expiry: 06th June 2024

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