HENNISS Basic Adult Surgery Set - Indonesia BPOM Medical Device Registration
HENNISS Basic Adult Surgery Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603111595. The device is manufactured by A. HENNISS. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MANDIRI JAYA MEDIKA.
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Risk Classification
Product Class
Kelas : 1
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
Mar 15, 2022
Expiry Date
Nov 08, 2026
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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