FIEGERT CO2 Insufflator - Indonesia BPOM Medical Device Registration
FIEGERT CO2 Insufflator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801310412. The device is manufactured by FIEGERT ENDOTECH MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRIMARY WORKS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FIEGERT ENDOTECH MEDIZINTECHNIK GMBH.Country of Origin
Germany
Authorized Representative
PT. PRIMARY WORKSAR Address
Daan Mogot Arcadia Blok F.1/8A-8B Jl. Daan Mogot Km 21, Kelurahan Batu Ceper
Registration Date
Aug 31, 2021
Expiry Date
Dec 31, 2025
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
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