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EXCOM HYBRID 1 - Indonesia BPOM Medical Device Registration

EXCOM HYBRID 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605520024. The device is manufactured by METASYS MEDIZINTECHNIK GMBH from Austria, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ANDINI SARANA.

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
EXCOM HYBRID 1
Analysis ID: AKL 10605520024

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Austria

Authorized Representative

ANDINI SARANA

AR Address

JL. Rawa Sumur III Kav. III Blok DD 11, Kawasan Industri Pulogadung

Registration Date

Jan 15, 2025

Expiry Date

Jul 12, 2029

Product Type

Other Dental Equipment

Dental operative unit and accessories.

Non Radiation Electromedics

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