FUJIFILM Medwork Polypectomy Snare - Indonesia BPOM Medical Device Registration
FUJIFILM Medwork Polypectomy Snare is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804420064. The device is manufactured by FUJIFILM MEDWORK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDISON JAYA RAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FUJIFILM MEDWORK GMBH.Country of Origin
Germany
Authorized Representative
PT. MEDISON JAYA RAYAAR Address
JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN
Registration Date
Nov 18, 2024
Expiry Date
Dec 31, 2029
Product Type
Gastroenterology-Surgical Urology Equipment
Endoscopic electrosurgical unit and accessories.
Non Electromedic Sterile
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