ESPF/XL

Organization name

ICOGUANTI S.p.A.

SRN

IT-MF-000053804

Manufacturer status

Active

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• CW129

  Contiene lattice di gomma naturale che può causare reazioni allergiche compreso lo shock anafilattico. Contiene potenziali allergeni che possono causare allergie di tipo IV.

Primary placement in Italy; available across 5 countries total.

Trade name

not provided

UDI-DI code

08005830002233

Basic UDI-DI

8005830GLPFYN

Reference / catalog number

ESPF/XL

Issuing entity

GS1

Risk category

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

100

Additional product description

Guanto Medicale Monouso da Esame a base di lattice di gomma naturale, senza polvere non sterile.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 240–250 MU50

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• T010201LATEX EXAMINATION / TREATMENT GLOVES