DIESSE Cube 30 Touch - Indonesia BPOM Medical Device Registration

DIESSE Cube 30 Touch is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10205024920. 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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BPOM Registered

Risk Class Kelas Resiko : A

DIESSE Cube 30 Touch

Analysis ID: AKL 10205024920

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

DIESSE DIAGNOSTICA SENESE S.P.A

Country of Origin

Italy

Authorized Representative

ABADINUSA USAHASEMESTA

AR Address

Jalan Raden Saleh No. 45 G

Registration Date

Aug 31, 2020

Expiry Date

May 20, 2025

Product Type

Automatic and Semi-Automatic Hematology Equipment

Automated sedimentation rate device.

Invitro Diagnostics

DJ Fang

MedTech Regulatory Expert

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