PRIMELINE Pro - Indonesia BPOM Medical Device Registration
PRIMELINE Pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903718451. The device is manufactured by AESCULAP AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AESCULAP AG.Country of Origin
Germany
Authorized Representative
B. BRAUN MEDICAL INDONESIAAR Address
Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan
Registration Date
Apr 06, 2023
Expiry Date
Nov 18, 2026
Product Type
General Hospital Equipment and Other Individuals
Sterilization wrap.
Non Electromedic Non Sterile
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