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RELYX Temp E - Indonesia BPOM Medical Device Registration

RELYX Temp E is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602613462. The device is manufactured by 3M DEUTSCLAND GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. 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 : C
RELYX Temp E
Analysis ID: AKL 20602613462

Risk Classification

Kelas Resiko : C

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

Apr 16, 2021

Expiry Date

Sep 25, 2025

Product Type

Prosthetic Dental Equipment

Dental cement

Non Electromedic Non Sterile

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