RUDOLF Gastro Intestinal Instrument Set - Indonesia BPOM Medical Device Registration
RUDOLF Gastro Intestinal Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10803502800. 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.
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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
Registration Date
Jul 02, 2020
Expiry Date
Dec 31, 2024
Product Type
Gastroenterology-Surgical Urology Equipment
Manual gastroenterology-urology surgical instrument and accessories.
Non Electromedic Non Sterile
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