CROSSFIX II Disposable Procedure Kit - Indonesia BPOM Medical Device Registration
CROSSFIX II Disposable Procedure Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303913167. The device is manufactured by CAYENNE MEDICAL, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. KALMED SEJAHTERA INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CAYENNE MEDICAL, INC.Country of Origin
United States
Authorized Representative
PT. KALMED SEJAHTERA INDONESIAAR Address
Jl. TMII Pintu II No. 2, RT 006 RW 004,
Registration Date
Apr 21, 2022
Expiry Date
Dec 08, 2026
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Sterile
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