RUDOLF Adult Basic Instrument Set - Indonesia BPOM Medical Device Registration
RUDOLF Adult Basic Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603502502. 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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
RUDOLF MEDICAL GMBH + CO. KG.Country of Origin
Germany
Authorized Representative
PT. GRAHA ISMAYAAR Address
Jalan Sultan Iskandar Muda Kav. 24 Arteri Pondok Indah
Registration Date
Dec 13, 2024
Expiry Date
Jul 10, 2028
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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