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3M ESPE Express XT Putty Soft - Indonesia BPOM Medical Device Registration

3M ESPE Express XT Putty Soft is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420198. 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 COBRA DENTAL INDONESIA.

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 Express XT Putty Soft
Analysis ID: AKL 20602420198

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

COBRA DENTAL INDONESIA

AR Address

Jl. Pakuningratan No. 69

Registration Date

May 07, 2024

Expiry Date

Aug 30, 2028

Product Type

Prosthetic Dental Equipment

Impression material.

Non Electromedic Non Sterile

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