RUDOLF ENT Examination Set - Indonesia BPOM Medical Device Registration
RUDOLF ENT Examination Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703026266. 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
Feb 02, 2024
Expiry Date
Jul 10, 2028
Product Type
Ear, Nose and Throat Surgical Equipment
Ear, nose, and throat manual surgical instrument.
Non Electromedic Non Sterile
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