DIESTRO ISE Calibrating KIT - Indonesia BPOM Medical Device Registration
DIESTRO ISE Calibrating KIT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101818565. The device is manufactured by JS MEDICINA ELECTRONICA S.R.L. from Argentina, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTISERA INDOSA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
JS MEDICINA ELECTRONICA S.R.L.Country of Origin
Argentina
Authorized Representative
PT. MULTISERA INDOSAAR Address
Jl. Jend. Sudirman No. 689 RT 21 RW 007
Registration Date
Feb 05, 2025
Expiry Date
Jan 12, 2028
Product Type
Clinical Chemistry Test System
Calibrator (cair)
Invitro Diagnostics
DIESTRO Calibrating Solutions Pack
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