CORINA Silicone Rubber Uterine Drug-Eluting Stent System - Indonesia BPOM Medical Device Registration
CORINA Silicone Rubber Uterine Drug-Eluting Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31104420354. The device is manufactured by PUYI (SHANGHAI) BIOTECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
PUYI (SHANGHAI) BIOTECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Nov 03, 2024
Expiry Date
Mar 12, 2027
Product Type
Therapeutic Obstetric and Gynecological Equipment
Uterine drug eluting stent
Non Electromedic Sterile
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