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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
GRIFF IVD LTD.Country of Origin
United Kingdom
Authorized Representative
PT. MACROCITRA ARDANASEJATIAR 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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RIGHTSIGN HAV Rapid Test Cassette (Serum/Plasma)
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RIGHTSIGN HCV Rapid Test Cassette (Serum/Plasma)
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RIGHTSIGN HBsAg Rapid Test Cassette (Serum/Plasma)
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RIGHTSIGN AMP Rapid Test Strip (Urine)
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RIGHTSIGN AMP Rapid Test Cassette (Urine)
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RIGHTSIGN THC Rapid Test Strip (Urine)
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