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RegenKit-ATS-T - Indonesia BPOM Medical Device Registration

RegenKit-ATS-T is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320616. The device is manufactured by REGEN LAB SA. from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is 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 : C
RegenKit-ATS-T
Analysis ID: AKL 20209320616

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

REGEN LAB SA.

Country of Origin

Switzerland

Authorized Representative

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

Sep 07, 2023

Expiry Date

Sep 29, 2027

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Automated blood cell separator

Non Electromedic Non Sterile

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