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3M TEGADERM Transparent Film Roll - Indonesia BPOM Medical Device Registration

3M TEGADERM Transparent Film Roll is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603514669. The device is manufactured by 3M DEUTSCHLAND GMBH/MEDICAL MANUFACTURING KAMEN from Germany, and is classified as Risk Class Kelas Resiko : A. 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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Risk Class Kelas Resiko : A
3M TEGADERM Transparent Film Roll
Analysis ID: AKL 11603514669

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

3M INDONESIA IMPORTAMA

AR Address

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

Registration Date

May 28, 2020

Expiry Date

Jan 31, 2024

Product Type

Surgical Equipment

Occlusive wound dressing.

Non Electromedic Non Sterile

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