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RUDOLF IUD Instrument SET - Indonesia BPOM Medical Device Registration

RUDOLF IUD Instrument SET is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103917741. The device is manufactured by RUDOLF MEDICAL, GMB + CO., KG, GERMANY from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is GRAHA ISMAYA.

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
RUDOLF IUD Instrument SET
Analysis ID: AKL 11103917741

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

GRAHA ISMAYA

AR Address

JALAN SULTAN ISKANDAR MUDA KAV 24

Registration Date

Nov 29, 2019

Expiry Date

Jan 17, 2024

Product Type

Surgical Obstetric and Gynaecological Equipment

Obstetric-gynecologic general manual instrument.

Non Electromedic Non Sterile

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