330048055 5.5

Organization name

Ansell Healthcare Europe NV

SRN

BE-MF-000000691

Manufacturer status

Active

4 warnings recorded — scroll inside the panel to see all entries.

• CW001

  EUDAMED did not publish a description for this code.
• CW007

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.
• CW011

  Product is made from natural rubber latex which can cause allergic reactions

Primary placement in Belgium; available across 32 countries total.

Trade name

not provided

UDI-DI code

15414566480558

Basic UDI-DI

5414566GLAT33004862

Reference / catalog number

330048055 5.5

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

https://www.ansell.com/gb/en/products/gammex-latex

Clinical sizes

No clinical sizes registered for this device.

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

• T01010102NON-POWDERED LATEX SURGICAL GLOVES