GEISTER Basic for Adult - Indonesia BPOM Medical Device Registration
GEISTER Basic for Adult is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603213032. The device is manufactured by GEISTER MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDTEK.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GEISTER MEDIZINTECHNIK GMBH.Country of Origin
Germany
Authorized Representative
PT. MEDTEKAR Address
DELTA BUILDING BLOK A-11, C-1 & C-2, JL. SURYOPRANOTO NO.1-9, RT/RW 004/007
Registration Date
Oct 31, 2024
Expiry Date
Mar 01, 2027
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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