ClearPetra Urological Guide Wire - Indonesia BPOM Medical Device Registration
ClearPetra Urological Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320842. The device is manufactured by WELL LEAD MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SOMETECH NEW Zealand.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WELL LEAD MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. SOMETECH NEW ZealandAR Address
AKR Tower Lantai 11 Unit 11G, Jl. Panjang No. 5
Registration Date
Jul 26, 2023
Expiry Date
Dec 07, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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