FUJITA Knife Instrument - Indonesia BPOM Medical Device Registration
FUJITA Knife Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603422508. The device is manufactured by CHARMANT INC. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is AKSATA MARGA MAKMUR.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CHARMANT INC.Country of Origin
Japan
Authorized Representative
AKSATA MARGA MAKMURAR Address
Foresta Business Loft 6 Unit 1, BSD City
Registration Date
Oct 25, 2024
Expiry Date
Jun 12, 2029
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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