FUJIFILM Medwork Foreign Body Forceps - Indonesia BPOM Medical Device Registration
FUJIFILM Medwork Foreign Body Forceps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801220180. The device is manufactured by FUJIFILM MEDWORK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDISON JAYA RAYA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
FUJIFILM MEDWORK GMBH.Country of Origin
Germany
Authorized Representative
MEDISON JAYA RAYAAR Address
JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN
Registration Date
Oct 28, 2024
Expiry Date
Dec 31, 2029
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
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