KLS Martin CMF Implant Part I - Sterile - Indonesia BPOM Medical Device Registration
KLS Martin CMF Implant Part I - Sterile is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302321094. The device is manufactured by GEBRÜDER MARTIN GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. IMEDITECH SOLUTIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GEBRÜDER MARTIN GMBH & CO. KG.Country of Origin
Germany
Authorized Representative
PT. IMEDITECH SOLUTIONS INDONESIAAR Address
Menara Palma 12th Floor, Jalan H.R Rasuna Said Kaveling 6 Blok X-2, Unit 1233 dan 1234
Registration Date
Dec 30, 2023
Expiry Date
Sep 22, 2027
Product Type
Prosthetic Orthopedic Equipment
Single/multiple component metallic bone fixation appliances and accessories.
Non Electromedic Sterile
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