MATRIX ™ Gel System Diluent - 2 LISS - Indonesia BPOM Medical Device Registration

MATRIX ™ Gel System Diluent - 2 LISS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208813120. The device is manufactured by TULIP DIAGNOSTICS [P] LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ZEFINDO DARYA MEGATAMA.

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BPOM Registered

Risk Class Kelas Resiko : B

MATRIX ™ Gel System Diluent - 2 LISS

Analysis ID: AKL 20208813120

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TULIP DIAGNOSTICS [P] LTD.

Country of Origin

India

Authorized Representative

PT. ZEFINDO DARYA MEGATAMA

AR Address

JL. JEMURSARI 329-331 B

Registration Date

Sep 26, 2023

Expiry Date

May 31, 2028

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

DJ Fang

MedTech Regulatory Expert

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