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FINECARE™ D-Dimer Control - Indonesia BPOM Medical Device Registration

FINECARE™ D-Dimer Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420337. The device is manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CIPTA VARIA KHARISMA UTAMA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
FINECARE™ D-Dimer Control
Analysis ID: AKL 20208420337

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

CIPTA VARIA KHARISMA UTAMA

AR Address

Jl. Utan Kayu Raya No. 105A Jakarta

Registration Date

Nov 01, 2024

Expiry Date

May 22, 2029

Product Type

Hematological Reagents

Hematology quality control mixture.

Invitro Diagnostics

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