KOSEN Ureteral Stent Set - Indonesia BPOM Medical Device Registration
KOSEN Ureteral Stent Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804320311. The device is manufactured by TIANCK MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. LUCKY MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TIANCK MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. LUCKY MEDICAL INDONESIAAR Address
Awana Town House Nomor 31, Jalan Mayjend Sutoyo
Registration Date
Aug 04, 2023
Expiry Date
May 11, 2028
Product Type
Gastroenterology-Surgical Urology Equipment
Ureteral stent.
Non Electromedic Sterile
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