VITAMED Dilatation and Curettage Set - Indonesia BPOM Medical Device Registration
VITAMED Dilatation and Curettage Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10804220069. The device is manufactured by VITAMED MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BETA MEDICAL.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
VITAMED MEDIZINTECHNIK GMBHCountry of Origin
Germany
Authorized Representative
PT. BETA MEDICALAR Address
Jl. Pangeran Antasari No. 212
Registration Date
Apr 03, 2023
Expiry Date
Dec 31, 2025
Product Type
Gastroenterology-Surgical Urology Equipment
Manual gastroenterology-urology surgical instrument and accessories.
Non Electromedic Non Sterile
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