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MEDITECH Medical Gas Regulator - Indonesia BPOM Medical Device Registration

MEDITECH Medical Gas Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402220050. The device is manufactured by B.N.O.S. MEDITECH LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SEKARGUNA 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
MEDITECH Medical Gas Regulator
Analysis ID: AKL 10402220050

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United Kingdom

Authorized Representative

SEKARGUNA MEDIKA

AR Address

jl.Ciputat Raya no 14 B.Pondok Pinang

Registration Date

Nov 08, 2022

Expiry Date

Jul 25, 2027

Product Type

Monitoring Anesthesia Equipment

Pressure regulator.

Non Electromedic Non Sterile

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