PROWLER™ Infusion Catheter - Indonesia BPOM Medical Device Registration
PROWLER™ Infusion Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501812719. The device is manufactured by CODMAN & SHURTLEFF, 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
CODMAN & SHURTLEFF, 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
Nov 29, 2021
Expiry Date
Jun 10, 2026
Product Type
Diagnostic Cardiology Equipment
Continuous flush catheter.
Non Electromedic Sterile
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