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DG Gel DC Scan - Indonesia BPOM Medical Device Registration

DG Gel DC Scan is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209420018. The device is manufactured by GRIFOLS AUSTRALIA PTY LTD from Australia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRISMED HOSLAB INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
DG Gel DC Scan
Analysis ID: AKL 20209420018

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Australia

Authorized Representative

PT. FRISMED HOSLAB INDONESIA

AR Address

Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321

Registration Date

Jan 11, 2024

Expiry Date

Mar 01, 2026

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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