RUDOLF Circumsision Instrument Set - Indonesia BPOM Medical Device Registration
RUDOLF Circumsision Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11104502515. 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 GRAHA ISMAYA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
RUDOLF MEDICAL GMBH + CO. KG.Country of Origin
Germany
Authorized Representative
GRAHA ISMAYAAR Address
Jalan Sultan Iskandar Muda Kav. 24 Arteri Pondok Indah
Registration Date
Nov 09, 2024
Expiry Date
Jul 10, 2028
Product Type
Surgical Obstetric and Gynaecological Equipment
Obstetric-gynecologic general manual instrument.
Non Electromedic Non Sterile
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