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Organization name
UDI-DI code
Reference / catalog number

30.3.32.01 L — Class I MDR by MCL Group srl

MD Atlas
MCL Group srl

EUDAMED last updated this device on Sep 17, 2025

30.3.32.01 L

805977798DCGLOVE3201GB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MCL Group srl
UDI-DI code: 08059777981915
Reference / catalog number: 30.3.32.01 L

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View device family (Basic UDI)

Manufacturer information

Organization name: MCL Group srl
SRN: IT-MF-000049484
Manufacturer status: Active

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70.7.18.06805977798DCMASK23F6On the market 30.3.17.03 XL805977798DCGLOVE1703GSOn the market 30.3.17.03 M805977798DCGLOVE1703GSOn the market 30.3.17.03805977798DCGLOVE1703GSOn the market 30.3.17.06 L805977798DCGLOVE1706GYOn 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.

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

Device identification

Trade name: not provided
UDI-DI code: 08059777981915
Basic UDI-DI: 805977798DCGLOVE3201GB
Reference / catalog number: 30.3.32.01 L
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: Guanto in nitrile, monouso, non sterile, privo di polvere lubrificante, clorinato internamente, forma anatomica, ambidestro, microruvido sulle dita, super sensibile, polso con bordino arrotolato, manichetta standard.
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)08059777981915

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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.

T01020204NITRILE 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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