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.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
RUDOLF MEDICAL, GMB + CO., KG, GERMANYCountry of Origin
Germany
Authorized Representative
GRAHA ISMAYAAR 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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