HENNISS Sectio Caesarean Instrument Set - Indonesia BPOM Medical Device Registration
HENNISS Sectio Caesarean Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21103610732. The device is manufactured by A. HENNISS. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MANDIRI JAYA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
A. HENNISS.Country of Origin
Germany
Authorized Representative
PT. MANDIRI JAYA MEDIKAAR Address
Graha Mas Fatmawati Blok B No. 20, Jl. RS. Fatmawati No. 71
Registration Date
Apr 14, 2022
Expiry Date
Nov 08, 2026
Product Type
Surgical Obstetric and Gynaecological Equipment
Obstetric-gynecologic specialized manual instrument.
Non Electromedic Non Sterile
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