REBOTEC Crutches - Indonesia BPOM Medical Device Registration
REBOTEC Crutches is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402420072. The device is manufactured by REBOTEC REHABILITATIONMITTEL GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DAYA PRIMA MANDIRI JAYA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
REBOTEC REHABILITATIONMITTEL GMBH.Country of Origin
Germany
Authorized Representative
PT. DAYA PRIMA MANDIRI JAYAAR Address
JL. KALIGARANG 1A SEMARANG
Registration Date
Mar 13, 2024
Expiry Date
Dec 31, 2028
Product Type
Prosthetic Physical Health Equipment
Crutch
Non Electromedic Non Sterile
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