MEICEN Baseplate - Indonesia BPOM Medical Device Registration
MEICEN Baseplate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11501123590. The device is manufactured by GUANGZHOU RENFU MEDICAL EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GUANGZHOU RENFU MEDICAL EQUIPMENT CO., LTD.Country of Origin
China
Authorized Representative
PT. TRANSMEDIC INDONESIAAR Address
PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137
Registration Date
Aug 09, 2021
Expiry Date
Dec 31, 2024
Product Type
Diagnostic Radiology Equipment
Radiographic head holder.
Non Electromedic Non Sterile
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