GIMMI Uterus Manipulator - Indonesia BPOM Medical Device Registration
GIMMI Uterus Manipulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21103320621. The device is manufactured by GIMMI GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEGASETIA AMORA KARSA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GIMMI GMBHCountry of Origin
Germany
Authorized Representative
MEGASETIA AMORA KARSAAR Address
JL. PARADISE TIMUR RAYA BLOK F-21 N0. 54
Registration Date
Oct 25, 2023
Expiry Date
Apr 01, 2028
Product Type
Surgical Obstetric and Gynaecological Equipment
Obstetric-gynecologic specialized manual instrument.
Non Electromedic Non Sterile
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