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KERR HARMONIZE - Indonesia BPOM Medical Device Registration

KERR HARMONIZE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420432. The device is manufactured by KERR ITALIA, S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TIGASATU MEDIKA SOLUSINDO.

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
KERR HARMONIZE
Analysis ID: AKL 20602420432

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

TIGASATU MEDIKA SOLUSINDO

AR Address

Karawaci Office Park, Jalan Imam Bonjol, Ruko Finangsia Blok H 53, Prov. Banten, Kota Tangerang, Kec. Cibodas, Kel. Panunggangan Barat

Registration Date

Nov 01, 2024

Expiry Date

Jan 26, 2027

Product Type

Prosthetic Dental Equipment

Tooth shade resin material.

Non Electromedic Non Sterile

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