DIESSE Vacu-Tec Cuvette L - Indonesia BPOM Medical Device Registration
DIESSE Vacu-Tec Cuvette L is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101113298. The device is manufactured by DIESSE DIAGNOSTICA SENESE S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ABADINUSA USAHASEMESTA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIESSE DIAGNOSTICA SENESE S.P.A.Country of Origin
Italy
Authorized Representative
PT. ABADINUSA USAHASEMESTAAR Address
Jalan Raden Saleh No. 45 G
Registration Date
Jun 17, 2020
Expiry Date
May 20, 2025
Product Type
Clinical Chemistry Test System
Blood specimen collection device
Invitro Diagnostics
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