Ambu® Subdermal Corkscrew

Organization name

Technomed Europe

SRN

NL-MF-000000064

Manufacturer status

Active

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

• CW027

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

  EUDAMED did not publish a description for this code.
• CW001

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

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

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

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

  EUDAMED did not publish a description for this code.

Primary placement in Netherlands; available across 32 countries total.

Trade name

Ambu® Subdermal Corkscrew

UDI-DI code

08720791370862

Basic UDI-DI

B-08720791370862

Reference / catalog number

74720-60/24

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

corkscrew 2.0m wire 4x6 colors 24pcs

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

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

• N01010202EEG EXTRACRANIC ELECTRODES