GENGIGEL Forte Gel - Indonesia BPOM Medical Device Registration
GENGIGEL Forte Gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325351. The device is manufactured by RICERFARMA SRL from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ISCO LOGISTICS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RICERFARMA SRLCountry of Origin
Italy
Authorized Representative
PT. ISCO LOGISTICS INDONESIAAR Address
JL. H.R. MOCH. MANGUNDIPROJO NO. 1A
Registration Date
Oct 27, 2023
Expiry Date
Jun 06, 2028
Product Type
Surgical Equipment
Hydrogel wound dressing and burn dressing.
Non Electromedic Non Sterile
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