Pure Global

MATTES Dilation & Curettage Set - Indonesia BPOM Medical Device Registration

MATTES Dilation & Curettage Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103220145. The device is manufactured by MATTES INSTRUMENTE GMBH MEDIZINTECHNIK. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ARTHA MEDIKA SENTOSA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
MATTES Dilation & Curettage Set
Analysis ID: AKL 11103220145

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. ARTHA MEDIKA SENTOSA

AR Address

Ruko Rose Garden 5 Nomor 115, Grand Galxy City, Desa/Kelurahan Jakasetia, Kec. Bekasi Selatan, Kota Bekasi, Provinsi Jawa Barat, Kode Pos: 17147

Registration Date

Jun 21, 2022

Expiry Date

Mar 30, 2027

Product Type

Surgical Obstetric and Gynaecological Equipment

Obstetric-gynecologic general manual instrument.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing