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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

COD471023 — 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

COD471023

803258463T01020299XP

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: 08032584639255
Reference / catalog number: COD471023

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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

COD63001402803258463T03993SOn the market COD05MSK403803258463T03993SOn the market COD63148060803258463T03993SOn the market COD63001600803258463T03993SOn the market COD63001503803258463T03993SOn 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: 08032584639255
Basic UDI-DI: 803258463T01020299XP
Reference / catalog number: COD471023
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: 200
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

EMDN nomenclature code(s)

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

T01020299SYNTHETIC EXAMINATION / TREATMENT GLOVES - OTHER

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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