VERION™ REFERENCE Unit - Indonesia BPOM Medical Device Registration
VERION™ REFERENCE Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201815147. The device is manufactured by WAVELIGHT GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BINASUKSES CANTEEN.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
WAVELIGHT GMBH.Country of Origin
Germany
Authorized Representative
PT. BINASUKSES CANTEENAR Address
Jl. Pulo Kambing II No. 26 Kawasan Industri Pulogadung, Kel. Jatinegara, Kec. Cakung, Kota Adm. Jakarta Timur, Provinsi DKI Jakarta, Kode Pos 13930
Registration Date
Nov 15, 2024
Expiry Date
Jul 01, 2026
Product Type
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