MOLLER Bone Biopsy Cannula - Indonesia BPOM Medical Device Registration
MOLLER Bone Biopsy Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801124520. The device is manufactured by MOLLER MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDISON JAYA RAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MOLLER MEDICAL GMBHCountry of Origin
Germany
Authorized Representative
PT. MEDISON JAYA RAYAAR Address
JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN
Registration Date
Aug 29, 2022
Expiry Date
Jun 03, 2027
Product Type
Diagnostic Gastroenterology-Urology Equipment
Gastroenterology-urology biopsy instrument
Non Electromedic Sterile
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