GENGIGEL Teething Gel - Indonesia BPOM Medical Device Registration
GENGIGEL Teething Gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603423000. The device is manufactured by RICERFARMA SRL from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ISCO LOGISTICS INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
RICERFARMA SRLCountry of Origin
Italy
Authorized Representative
ISCO LOGISTICS INDONESIAAR Address
JL. H.R. MOCH. MANGUNDIPROJO NO. 1A
Registration Date
Dec 30, 2024
Expiry Date
Sep 30, 2029
Product Type
Surgical Equipment
Hydrogel wound dressing and burn dressing.
Non Electromedic Non Sterile
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