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KETTENBACH Identium Medium - Indonesia BPOM Medical Device Registration

KETTENBACH Identium Medium is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602812255. The device is manufactured by KETTENBACH GMBH & CO. Medical history. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FONDACO JAYATAMA.

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
KETTENBACH Identium Medium
Analysis ID: AKL 20602812255

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. FONDACO JAYATAMA

AR Address

APL Tower Podomoro City Lantai 27 T1, T2, T5, Jln Letjen S. Parman Kavling 28

Registration Date

Nov 12, 2024

Expiry Date

Dec 02, 2025

Product Type

Prosthetic Dental Equipment

Impression material.

Non Electromedic Non Sterile

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