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REGENKIT -BCT - Indonesia BPOM Medical Device Registration

REGENKIT -BCT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101313805. The device is manufactured by REGEN LAB SA. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. I-TECH LAFACOS.

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
REGENKIT -BCT
Analysis ID: AKL 20101313805

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

REGEN LAB SA.

Country of Origin

Switzerland

Authorized Representative

PT. I-TECH LAFACOS

AR Address

Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih

Registration Date

Nov 25, 2022

Expiry Date

Sep 29, 2027

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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