Quality certificates & policy documents

Medfor's CE certificate with extension letter

Medfor's class IIa MDD products conform to Directive 93/42/EEC on medical devices, with extension letter from SGS. Updated 30 Jan 2024.

Medfor's UKCA certificate

Medfor's class IIa MDD products conform to Regulation MDR 2002. Updated 31 Jan 2024.

Medfor's ISO 13485:2016 certificate (DNV)

Valid from 19 March 2026 until 16 March 2029. Updated 12 May 2026.

Medfor's MDR certificate (DNV)

Valid 29 April 2031. Updated 12 May 2026.

EU Declaration of Conformity (MDD products)

Covers Medfor's MDD (in vivo) products intended for storage of human tissue prior to transplant use. Issue 18 (15 Jan 2024).

EU Declaration of Conformity (IVD products)

Covers all Medfor's IVD (in vitro diagnostic) products intended for laboratory and general purpose use. Issue 5, 13 Sep 2024.

UK Declaration of Conformity (MDD products)

Covers Medfor's MDD (in vivo) products intended for storage of human tissue prior to transplant use. Issue 1 (15 Jan 2024).

UK Declaration of Conformity (IVD products)

Covers all Medfor's IVD (in vitro diagnostic) products intended for laboratory and general purpose use. Issue 3, 13 Sep 2024.

BSE Statement (PDF 134 KB)

Next due for review in June 2026.

Medfor's Terms and Conditions of Sale (PDF 54 KB)

Credit Account application form (PDF 153 KB)

Medfor's Health & Saftey Policy

Medfor's Product & Employer Liability Insurance

Summary of Medfor's insurance cover for the period to 18/7/26.

Medfor's Modern Slavery Policy

Medfor's Equal Opportunity Policy