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DIAGAST Anti-D (RH1) IgM I - Indonesia BPOM Medical Device Registration

DIAGAST Anti-D (RH1) IgM I is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209806661. The device is manufactured by DIAGAST INC. from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDQUEST JAYA GLOBAL.

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
DIAGAST Anti-D (RH1) IgM I
Analysis ID: AKL 20209806661

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

DIAGAST INC.

Country of Origin

France

Authorized Representative

PT. MEDQUEST JAYA GLOBAL

AR Address

Menara Salemba Lantai 6 Jl. Salemba Raya Kav. 5 - 5A

Registration Date

Feb 13, 2023

Expiry Date

Sep 30, 2027

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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