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RUDOLF Tonsilectomy Instrument Set - Indonesia BPOM Medical Device Registration

RUDOLF Tonsilectomy Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703700096. The device is manufactured by RUDOLF MEDICAL GMBH. + CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. 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 Tonsilectomy Instrument Set
Analysis ID: AKL 10703700096

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. GRAHA ISMAYA

AR Address

JALAN SULTAN ISKANDAR MUDA KAV 24

Registration Date

Sep 17, 2020

Expiry Date

Jan 17, 2024

Product Type

Ear, Nose and Throat Surgical Equipment

Ear, nose, and throat manual surgical instrument.

Non Electromedic Non Sterile

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