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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

DTNT/L — Class I MDR by ICOGUANTI S.p.A.

MD Atlas
ICOGUANTI S.p.A.

EUDAMED last updated this device on May 15, 2026

DTNT/L

8005830GNPFYY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ICOGUANTI S.p.A.
UDI-DI code: 08005830011587
Reference / catalog number: DTNT/L

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View device family (Basic UDI)

Manufacturer information

Organization name: ICOGUANTI S.p.A.
SRN: IT-MF-000053804
Manufacturer status: Active

Related devices

HCN/L8005830GNPFYYOn the market HCN/M8005830GNPFYYOn the market HCN/S8005830GNPFYYOn the market ENPF/XS8005830GNPFYYOn the market ESMS/L8005830GLPPZAOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW129
Contiene potenziali allergeni che possono causare allergie di tipo IV.

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Market distribution

Primary placement in Italy; available across 2 countries total.

Country	On market since	Until
ItalyPrimary placement	Mar 25, 2022	Still on market
Spain	Mar 25, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08005830011587
Basic UDI-DI: 8005830GNPFYY
Reference / catalog number: DTNT/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 Medicale Monouso da Esame a base di nitrile (gomma sintetica) senza polvere non sterile.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 240–250 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08005830011587

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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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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.