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INSIGHT DOA PANEL 6.1 DEVICE - Indonesia BPOM Medical Device Registration

INSIGHT DOA PANEL 6.1 DEVICE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103320393. The device is manufactured by TULIP DIAGNOSTICS (P) LTD from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAVIA CITRA LESTARI.

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BPOM Registered
Risk Class Kelas Resiko : C
INSIGHT DOA PANEL 6.1 DEVICE
Analysis ID: AKL 20103320393

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. GRAVIA CITRA LESTARI

AR Address

Komplek Rukan Gading Bukit Indah Blok C15 Jl. Bukit Gading Raya

Registration Date

Jun 01, 2023

Expiry Date

Nov 23, 2027

Product Type

Clinical Toxicology Test System

Multi parameter clinical toxicology test system

Invitro Diagnostics

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