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SILAGUM PuTTY Standard - Indonesia BPOM Medical Device Registration

SILAGUM PuTTY Standard is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602511903. The device is manufactured by DMG CHEMISH-PHARMAZEUTISCHE FABRIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is THOMASONG NIRMALA.

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
SILAGUM PuTTY Standard

SILAGUM Putty Standar

Analysis ID: AKL 20602511903

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

THOMASONG NIRMALA

AR Address

Jl. AM. Sangaji No. 20A

Registration Date

Feb 12, 2024

Expiry Date

Dec 31, 2026

Product Type

Prosthetic Dental Equipment

Impression material.

Non Electromedic Non Sterile

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