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3M AVAGARD - Indonesia BPOM Medical Device Registration

3M AVAGARD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903021208. The device is manufactured by 3M COMPANY, 3M HEALTH CARE from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 3M INDONESIA IMPORTAMA.

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
3M AVAGARD
Analysis ID: AKL 20903021208

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

3M INDONESIA IMPORTAMA

AR Address

KAWASAN PERKANTORAN HIJAU ARKADIA, TOWER F, LT.9, JL. TB. SIMATUPANG KAV. 88

Registration Date

Mar 17, 2020

Expiry Date

Jan 31, 2024

Product Type

General Hospital Equipment and Other Individuals

General purpose disinfectants.

Non Electromedic Non Sterile

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