Pursuant to Regulation (EU) 2017/745 on Medical Devices, Annex IX Chapters I and III
(Class IIa and Class IIb Devices)
No. G10 012998 0012 Rev. 02
SRN Manufacturer: DE-MF-000012632
Full Quality Assurance System
Directive 93/42/EEC on Medical Devices (MDD), Annex II excluding (4)
(Devices in Class IIa, IIb or III)
No. G1 012998 0010 Rev. 00
No. Q5 012998 0011 Rev. 01