Pure Global

LIFOTRONlC Syphilis (eCLlA) - Indonesia BPOM Medical Device Registration

LIFOTRONlC Syphilis (eCLlA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420006. The device is manufactured by SHENZHEN LIFOTRONIC TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. LIFOTRONIC TECHNOLOGY INDONESIA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
LIFOTRONlC Syphilis (eCLlA)
Analysis ID: AKL 20303420006

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. LIFOTRONIC TECHNOLOGY INDONESIA

AR Address

Ruko South Goldfinch Blok SGA No. 17, Jl. Spring Boulevard, Kode Pos 15322, Kel. Cihuni, Kec. Pagedangan, Kab. Tangerang, Provinsi Banten

Registration Date

Jan 05, 2024

Expiry Date

Mar 13, 2028

Product Type

Serological Reagents

Treponema pallidum treponemal test reagents.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing