DIESSE VES MATIC Original - Indonesia BPOM Medical Device Registration
DIESSE VES MATIC Original is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10205320543. The device is manufactured by DIESSE DIAGNOSTICA SENESE S.P.A from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ABADINUSA USAHASEMESTA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
DIESSE DIAGNOSTICA SENESE S.P.ACountry of Origin
Italy
Authorized Representative
ABADINUSA USAHASEMESTAAR Address
Jalan Raden Saleh No. 45 G
Registration Date
Dec 04, 2023
Expiry Date
May 20, 2025
Product Type
Automatic and Semi-Automatic Hematology Equipment
Automated sedimentation rate device.
Invitro Diagnostics
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