KLS Martin CMF Instrument Set Part II - Indonesia BPOM Medical Device Registration
KLS Martin CMF Instrument Set Part II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420008. The device is manufactured by GEBRÜDER MARTIN GMBH & CO. KG from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is IMEDITECH SOLUTIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GEBRÜDER MARTIN GMBH & CO. KGCountry of Origin
Germany
Authorized Representative
IMEDITECH SOLUTIONS INDONESIAAR Address
Menara Palma 12th Floor, Jalan H.R Rasuna Said Kaveling 6 Blok X-2, Unit 1233 dan 1234
Registration Date
Jan 09, 2024
Expiry Date
Sep 22, 2027
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
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KLS Martin CMF Instrument -Part I
KLS Martin Twist Drill
KLS Martin CMF Instruments Set - Part III
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