DEOX Oxygen Barrier Sollution - Indonesia BPOM Medical Device Registration
DEOX Oxygen Barrier Sollution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420267. The device is manufactured by ULTRADENT PRODUCTS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FONDACO JAYATAMA.
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
ULTRADENT PRODUCTS, INC.Country of Origin
United States
Authorized Representative
PT. FONDACO JAYATAMAAR Address
Agung Podomoro Land Tower, Podomoro City Lt. 27 T1, T2, T5 Jl. Letnan Jendral Siswondo Parman Kav. 28 Kel. Tanjung Duren Selatan, Kec. Grogol Petamburan, Jakarta Barat, DKI Jakarta
Registration Date
Jun 24, 2024
Expiry Date
Apr 18, 2029
Product Type
Prosthetic Dental Equipment
Dental cement.
Non Electromedic Non Sterile
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