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FRESENIUS Composeal Mobilea II - Indonesia BPOM Medical Device Registration

FRESENIUS Composeal Mobilea II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209410468. The device is manufactured by FRESENIUS HEMOCARE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FRESENIUS KABI 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.

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BPOM Registered
Risk Class Kelas Resiko : A
FRESENIUS Composeal Mobilea II
Analysis ID: AKL 10209410468

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. FRESENIUS KABI INDONESIA

AR Address

Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870

Registration Date

May 26, 2023

Expiry Date

Dec 19, 2027

Product Type

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

Heat-sealing device.

Non Radiation Electromedics

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