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TUBEX TF - Indonesia BPOM Medical Device Registration

TUBEX TF is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303020317. The device is manufactured by IDL BIOTECH AB from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BRIDGE TWO.

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
TUBEX TF
Analysis ID: AKL 20303020317

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

IDL BIOTECH AB

Country of Origin

Sweden

Authorized Representative

BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Apr 24, 2024

Expiry Date

Mar 01, 2029

Product Type

Serological Reagents

Salmonella spp. serological reagents.

Invitro Diagnostics

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