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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

Discs for antimicrobial… — IVDR Class A IVDR

MD Atlas
Tody Laboratories Med SRL

EUDAMED last updated this device on Oct 25, 2024

Discs for antimicrobial susceptibility testing Clindamycin, CD, 10mcg

594067440SUSCEPT.DISCSZK

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Tody Laboratories Med SRL
UDI-DI code: 05940674400681
Reference / catalog number: C39SD1072

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View device family (Basic UDI)

Manufacturer information

Organization name: Tody Laboratories Med SRL
SRN: RO-MF-000037201
Manufacturer status: Active

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.
CW133
EUDAMED did not publish a description for this code.
CW168
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: Discs for antimicrobial susceptibility testing Clindamycin, CD, 10mcg
UDI-DI code: 05940674400681
Basic UDI-DI: 594067440SUSCEPT.DISCSZK
Reference / catalog number: C39SD1072
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05940674400681

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

W0104080502IMPREGNATED DISKS, MULTI-DISKS & TABLETS

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Certificates

No 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.