FAZZINI Dilation and Curetage Set - Indonesia BPOM Medical Device Registration
FAZZINI Dilation and Curetage Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103915153. The device is manufactured by FAZZINI S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is GEBANG SURYA HARAPAN.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FAZZINI S.R.L.Country of Origin
Italy
Authorized Representative
GEBANG SURYA HARAPANAR Address
Ruko Puri Botanical Junction Blok I 10 No. 1 Jl. Raya Joglo RT 007 RW 001 Kel. Joglo, Kec. Kembangan, Jakarta Barat
Registration Date
Nov 08, 2023
Expiry Date
Jan 01, 2027
Product Type
Surgical Obstetric and Gynaecological Equipment
Obstetric-gynecologic general manual instrument.
Non Electromedic Non Sterile
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