ACL Disposable Procedure Kit - Indonesia BPOM Medical Device Registration
ACL Disposable Procedure Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303020138. 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.TAMAN MINI PINTU 2 NO. 2, RT. 006 RW. 004
Registration Date
Aug 19, 2024
Expiry Date
Dec 08, 2026
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
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