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PRO-MED Obstetric-Gynecologic General Manual Instrument - Indonesia BPOM Medical Device Registration

PRO-MED Obstetric-Gynecologic General Manual Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103127178. The device is manufactured by PRO-MED INSTRUMENTE GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FIVE RELIABLE PARTNERS.

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 : A
PRO-MED Obstetric-Gynecologic General Manual Instrument
Analysis ID: AKL 11103127178

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. FIVE RELIABLE PARTNERS

AR Address

Graha Iskandarsyah, Lantai 10, Jln. Raya Sultan Iskandarsyah No. 66 C, Kel. Melawai, Kec. Kebayoran Baru, Kota Adm. Jakarta Selatan, Prop. DKI Jakarta

Registration Date

Nov 22, 2021

Expiry Date

Mar 23, 2026

Product Type

Surgical Obstetric and Gynaecological Equipment

Obstetric-gynecologic general manual instrument.

Non Electromedic Non Sterile

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