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ASTRA 3i Anaesthesia machine - Indonesia BPOM Medical Device Registration

ASTRA 3i Anaesthesia machine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403120297. The device is manufactured by OES MEDICAL LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SALSABIL RESA PRADANA.

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
ASTRA 3i Anaesthesia machine
Analysis ID: AKL 20403120297

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. SALSABIL RESA PRADANA

AR Address

Sentral Senayan II Office Tower Lt.16 Unit 216A Jl. Asia Afrika No.6 Jakarta Pusat

Registration Date

Mar 16, 2023

Expiry Date

Feb 09, 2028

Product Type

Therapeutic Anesthesia Equipment

Gas machine for anesthesia or analgesia.

Non Radiation Electromedics

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