REVMEDX Injectable Hemostatic Device - Indonesia BPOM Medical Device Registration
REVMEDX Injectable Hemostatic Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222421. The device is manufactured by REVMEDX, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RANAYA FAZZA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
REVMEDX, INC.Country of Origin
United States
Authorized Representative
PT. RANAYA FAZZA UTAMAAR Address
Graha Harapan Blok E14/12
Registration Date
Oct 10, 2022
Expiry Date
Sep 22, 2026
Product Type
Surgical Equipment
Nonabsorbable expandable hemostatic sponge for temporary internal use.
Non Electromedic Non Sterile
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