BELOTERO® Balance Lidocaine - Indonesia BPOM Medical Device Registration
BELOTERO® Balance Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602817999. The device is manufactured by ANTEIS S.A. (LONAY) from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. PHARMINDO LESTARI AWARD.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
ANTEIS S.A. (LONAY)Country of Origin
Switzerland
Authorized Representative
PT. PHARMINDO LESTARI AWARDAR Address
Jl. Boulevard BGR No. 1, Komplek Pergudangan BGR Gudang M, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara, DKI Jakarta
Registration Date
Jun 27, 2022
Expiry Date
Feb 14, 2027
Product Type
Prosthetic Surgical Equipment
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