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GAZELLE ™ Hb Variant Test Multipack - Indonesia BPOM Medical Device Registration

GAZELLE ™ Hb Variant Test Multipack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205320502. The device is manufactured by LAKSHMI LIFE SCIENCE PRIVATE LIMITED from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDQUEST JAYA GLOBAL.

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BPOM Registered
Risk Class Kelas Resiko : B
GAZELLE ™ Hb Variant Test Multipack
Analysis ID: AKL 20205320502

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. MEDQUEST JAYA GLOBAL

AR Address

MENARA SALEMBA LT.6 ZONE 1, Jalan SALEMBA RAYA KAV.5-5A

Registration Date

Oct 25, 2023

Expiry Date

Oct 26, 2027

Product Type

Automatic and Semi-Automatic Hematology Equipment

Automated hemoglobin system (for reagent & control)

Invitro Diagnostics

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