ACTI-LANCE Universal - 23G - Indonesia BPOM Medical Device Registration
ACTI-LANCE Universal - 23G is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603816849. The device is manufactured by HTL-STREFA S.A. from Poland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HTL-STREFA S.A.Country of Origin
Poland
Authorized Representative
BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Jan 22, 2025
Expiry Date
Nov 28, 2029
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Sterile
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