UROMED Ureteral Stent - Indonesia BPOM Medical Device Registration
UROMED Ureteral Stent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804815301. The device is manufactured by MANISH MEDI INNOVATION from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SINAR MULIA INDOMEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MANISH MEDI INNOVATIONCountry of Origin
India
Authorized Representative
PT. SINAR MULIA INDOMEDIKAAR Address
Jl. Sukamanah V No. 20
Registration Date
Jan 04, 2025
Expiry Date
Nov 30, 2025
Product Type
Gastroenterology-Surgical Urology Equipment
Ureteral stent.
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