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3M Elipar DeepCure-L - Indonesia BPOM Medical Device Registration

3M Elipar DeepCure-L is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605611885. The device is manufactured by 3M DEUTSCHLAND GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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 Elipar DeepCure-L
Analysis ID: AKL 20605611885

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. 3M INDONESIA IMPORTAMA

AR Address

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

Registration Date

Feb 01, 2021

Expiry Date

Sep 25, 2025

Product Type

Other Dental Equipment

Ultraviolet activator for polymerization.

Non Radiation Electromedics

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