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EUDAMED last updated this device on Oct 25, 2024
594067440SUSCEPT.DISCSZKPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Discs for antimicrobial susceptibility testing Azithromycin, AZM, 15mcg is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Tody Laboratories Med SRL. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →05940674401312Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →594067440SUSCEPT.DISCSZKC39SD1018UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →(01)05940674401312
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0104080502IMPREGNATED DISKS, MULTI-DISKS & TABLETS5 warnings recorded — scroll inside the panel to see all entries.
CW009CW007CW032CW133CW168Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
Primary placement in Spain; available across 1 country total.
Placed on the market in Spain; per-country availability dates not published.
RO-MF-000037201No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.594067440SUSCEPT.DISCSZKOn the marketDiscs for antimicrobial susceptibility testing Amikacin, AK, 10mcg594067440SUSCEPT.DISCSZKOn the marketDiscs for antimicrobial susceptibility testing Amikacin, AK, 30mcg594067440SUSCEPT.DISCSZKOn the marketDiscs for antimicrobial susceptibility testing Amoxycillin, AMX, 10mcg594067440SUSCEPT.DISCSZKOn the marketDiscs for antimicrobial susceptibility testing Amoxycillin, AMX, 25mcg594067440SUSCEPT.DISCSZKOn the market