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D-MACH Mobile Tube Sealer - Indonesia BPOM Medical Device Registration

D-MACH Mobile Tube Sealer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209420367. The device is manufactured by CENTRON CORPORATION from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MITRA BAHAGIA CITRA MEDIKA.

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
D-MACH Mobile Tube Sealer
Analysis ID: AKL 10209420367

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

PT. MITRA BAHAGIA CITRA MEDIKA

AR Address

JL.RAYA KALIRUNGKUT 27 BLOK C/63 KALIRUNGKUT

Registration Date

Sep 27, 2024

Expiry Date

Jul 01, 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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