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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

COD512022 — Class I MDR by CO.DI.SAN. COMMERCIO…

MD Atlas
CO.DI.SAN. COMMERCIO DISTRIBUZIONE SANITARI S.P.A.

EUDAMED last updated this device on May 13, 2026

COD512022

803258463T01020201WC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CO.DI.SAN. COMMERCIO DISTRIBUZIONE SANITARI S.P.A.
UDI-DI code: 08032584630917
Reference / catalog number: COD512022

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View device family (Basic UDI)

Manufacturer information

Organization name: CO.DI.SAN. COMMERCIO DISTRIBUZIONE SANITARI S.P.A.
SRN: IT-MF-000020492
Manufacturer status: Active

Related devices

CODPAN001805208622Y093399WLOn the market COD003154803258463A06030301KUOn the market COD001144803258463A06030301KUOn the market COD003540803258463A06030301KUOn the market COD001244803258463A06030301KUOn the market

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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08032584630917
Basic UDI-DI: 803258463T01020201WC
Reference / catalog number: COD512022
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 100
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)08032584630917

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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.

T010201LATEX EXAMINATION / TREATMENT GLOVES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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