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SUPRAMID - Indonesia BPOM Medical Device Registration

SUPRAMID is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603510215. 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 PT. 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.

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BPOM Registered
Risk Class Kelas Resiko : C
SUPRAMID
Analysis ID: AKL 21603510215

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. FA ANTARES MEDIKA

AR Address

RUKO GOLDEN BOULEVARD BLOK I NO.7

Registration Date

Mar 05, 2024

Expiry Date

Feb 11, 2029

Product Type

Surgical Equipment

Nonabsorbable polyamide surgical suture.

Non Electromedic Sterile

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