619002

Organization name

Bingold GmbH + Co. KG

SRN

DE-MF-000016561

Manufacturer status

Active

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

• CW010

  EUDAMED did not publish a description for this code.
• CW009

  EUDAMED did not publish a description for this code.
• CW020

  EUDAMED did not publish a description for this code.
• CW032

  EUDAMED did not publish a description for this code.

Primary placement in Germany; available across 1 country total.

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

Trade name

not provided

UDI-DI code

04004034619012

Basic UDI-DI

4004034LOC50G7

Reference / catalog number

619002

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

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• black
• M

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

• T010201LATEX EXAMINATION / TREATMENT GLOVES