ZEPF MEDICAL INSTRUMENTS is certified according to DIN ISO 9001/2008, 13485:2007, Annex II and V of the Directive 93/42/EWG and EN 46001. This guarantees the traceability of Zepf instruments from the molten steel to the finished product. Zepf meet the requirements and are registered in U.S. FDA as well as other food and drug safety administrations.

All Zepf products have the CE marking. All products which are higher than Class I are marked with the CE and the number of the "Notified Body ".