GREATBATCH PTFE Peelable introducer Kit - Indonesia BPOM Medical Device Registration
GREATBATCH PTFE Peelable introducer Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501321173. The device is manufactured by GREATBATCH MEDICAL, S. DE R.L. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GREATBATCH MEDICAL, S. DE R.L. DE C.V.Country of Origin
Mexico
Authorized Representative
TRANSMEDIC INDONESIAAR Address
PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137
Registration Date
Nov 27, 2023
Expiry Date
Aug 01, 2027
Product Type
Diagnostic Cardiology Equipment
Catheter introducer
Non Electromedic Sterile
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