SERAPID - Indonesia BPOM Medical Device Registration
SERAPID is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603510221. The device is manufactured by SERAG-WIESSNER GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FA ANTARES MEDIKA.
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
SERAG-WIESSNER GMBH & CO. KG.Country of Origin
Germany
Authorized Representative
FA ANTARES MEDIKAAR Address
RUKO GOLDEN BOULEVARD BLOK I NO.7
Registration Date
Jan 16, 2024
Expiry Date
Jan 12, 2029
Product Type
Surgical Equipment
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