CELSIUS FLTR Catheter - Indonesia BPOM Medical Device Registration
CELSIUS FLTR Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501915048. The device is manufactured by BIOSENSE WEBSTER INC. from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. JOHNSON & JOHNSON NEW ZEALAND.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOSENSE WEBSTER INC.Country of Origin
Mexico
Authorized Representative
PT. JOHNSON & JOHNSON NEW ZEALANDAR Address
K-Link Tower Lt. 12, Jln. Jend. Gatot Subroto Kav. 59 A
Registration Date
Jul 28, 2022
Expiry Date
Feb 22, 2027
Product Type
Diagnostic Cardiology Equipment
Electrode recording catheter or electrode recording probe.
Non Electromedic Sterile
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