VEINOPLUS® BACK - Indonesia BPOM Medical Device Registration
VEINOPLUS® BACK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403818718. The device is manufactured by AD REM TECHNOLOGY. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDONESIA GLOBAL MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AD REM TECHNOLOGY.Country of Origin
France
Authorized Representative
INDONESIA GLOBAL MEDIKAAR Address
APL Tower 16th floor, T9 Podomoro City, (Central Park) Jl. LetJend S. Parman Kav 28, Jakarta 11470 INDONESIA
Registration Date
Nov 22, 2022
Expiry Date
Jul 05, 2027
Product Type
Therapeutic Physical Health Equipment
Powered muscle stimulator.
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