ENDO - FLEX Stent Placement Set - Indonesia BPOM Medical Device Registration
ENDO - FLEX Stent Placement Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320835. The device is manufactured by ENDO - FLEX GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDISON JAYA RAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ENDO - FLEX GMBHCountry of Origin
Germany
Authorized Representative
MEDISON JAYA RAYAAR Address
JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN
Registration Date
Jul 25, 2023
Expiry Date
Aug 04, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Biliary catheter and accessories.
Non Electromedic Sterile
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