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ODAK Gel Card Centrifuge - Indonesia BPOM Medical Device Registration

ODAK Gel Card Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209220318. The device is manufactured by ISLAB BIOTECHNOLOGY MEDICAL MATERIAL HEALTH SPEED. SAN. VE TIC. A.S. from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PRIMA ALKESINDO NUSANTARA.

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
ODAK Gel Card Centrifuge
Analysis ID: AKL 20209220318

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PRIMA ALKESINDO NUSANTARA

AR Address

Jl. Bukit Gading Raya Blok C 12 - C 15 Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara

Registration Date

Nov 09, 2024

Expiry Date

Oct 04, 2029

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Automated blood grouping and antibody test system.

Invitro Diagnostics

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