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Certofix Trio Paed - Indonesia BPOM Medical Device Registration

Certofix Trio Paed is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902321721. The device is manufactured by B. BRAUN MELSUNGEN AG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.

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
Certofix Trio Paed
Analysis ID: AKL 20902321721

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

B. BRAUN MEDICAL INDONESIA

AR Address

Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan

Registration Date

Feb 27, 2023

Expiry Date

Jan 12, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular catheter.

Non Electromedic Sterile

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