CROSSFIX II Meniscal Repair Device - Indonesia BPOM Medical Device Registration
CROSSFIX II Meniscal Repair Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603913723. The device is manufactured by CAYENNE MEDICAL INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KALMED SEJAHTERA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
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 25, 2022
Expiry Date
Dec 08, 2026
Product Type
Surgical Equipment
Nonabsorbable poly(ethylene terephthalate) surgical suture.
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