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GRIFF TPHA 200T KIT - Indonesia BPOM Medical Device Registration

GRIFF TPHA 200T KIT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303127032. The device is manufactured by GRIFF IVD LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MACROCITRA ARDANASEJATI.

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 : C
GRIFF TPHA 200T KIT
Analysis ID: AKL 20303127032

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

GRIFF IVD LTD.

Country of Origin

United Kingdom

Authorized Representative

PT. MACROCITRA ARDANASEJATI

AR Address

Rukan Taman Meruya Blok M-65 Meruya Ilir - Jakarta Barat Telp. 021-5874575, Fax. 021-5874573

Registration Date

Nov 17, 2021

Expiry Date

Dec 31, 2025

Product Type

Serological Reagents

Treponema pallidum treponemal test reagents.

Invitro Diagnostics

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