GIMMI Reusable Trocar System - Indonesia BPOM Medical Device Registration
GIMMI Reusable Trocar System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501321084. 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 18, 2023
Expiry Date
Apr 01, 2028
Product Type
Diagnostic Cardiology Equipment
Barter.
Non Electromedic Non Sterile
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