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3M ESPE Relyx Ultimate Clicker - Indonesia BPOM Medical Device Registration

3M ESPE Relyx Ultimate Clicker is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602610085. 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 ESPE Relyx Ultimate Clicker
Analysis ID: AKL 20602610085

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

Dec 07, 2020

Expiry Date

Jul 14, 2025

Product Type

Prosthetic Dental Equipment

Dental cement.

Non Electromedic Non Sterile

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