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AMBU Mark IV Resuscitator - Indonesia BPOM Medical Device Registration

AMBU Mark IV Resuscitator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420216. The device is manufactured by AMBU., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is AMI MEDIKA 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 : B
AMBU Mark IV Resuscitator
Analysis ID: AKL 20403420216

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AMBU., LTD.

Country of Origin

China

Authorized Representative

AMI MEDIKA INDONESIA

AR Address

The Savoy B1-30, Jakarta Garden City Boulevard

Registration Date

Mar 13, 2024

Expiry Date

Aug 31, 2028

Product Type

Therapeutic Anesthesia Equipment

Manual emergency ventilator.

Non Electromedic Non Sterile

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