RUDOLF Partus Instrument Set - Indonesia BPOM Medical Device Registration
RUDOLF Partus Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21104502583. The device is manufactured by RUDOLF MEDICAL GMBH + CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GRAHA ISMAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RUDOLF MEDICAL GMBH + CO. KG.Country of Origin
Germany
Authorized Representative
PT. GRAHA ISMAYAAR Address
JALAN SULTAN ISKANDAR MUDA KAV 24
Registration Date
Sep 04, 2020
Expiry Date
Dec 31, 2024
Product Type
Surgical Obstetric and Gynaecological Equipment
Obstetric-gynecologic specialized manual instrument.
Non Electromedic Non Sterile
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