VIRTUE DX FT3 Reagent Kit - Indonesia BPOM Medical Device Registration

VIRTUE DX FT3 Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101323995. The device is manufactured by VIRTUE DIAGNOSTICS SUZHOU CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DARMA LABORA INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

VIRTUE DX FT3 Reagent Kit

Analysis ID: AKL 20101323995

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VIRTUE DIAGNOSTICS SUZHOU CO., LTD.

Country of Origin

China

Authorized Representative

PT. DARMA LABORA INDONESIA

AR Address

KAWASAN INDUSTRI JABABEKA 7, BLOK B3/B, DESA WANGUNHARJA

Registration Date

Oct 07, 2024

Expiry Date

Mar 02, 2028

Product Type

Clinical Chemistry Test System

Free thyroxine test system (kit & cair)

Invitro Diagnostics

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Other Products from VIRTUE DIAGNOSTICS SUZHOU CO., LTD.

Products from the same manufacturer (10 products)

VIRTUE DX FT3 Reagent Kit - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

DJ Fang

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