900668

Organization name

Helago-Pharma GmbH & Co. KG

SRN

DE-MF-000004933

Manufacturer status

Active

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

• CW129

  Enthält Dikaliumperoxodisulfat. Kann allergische Reaktionen hervorrufen.
• CW076

  EUDAMED did not publish a description for this code.
• CW082

  EUDAMED did not publish a description for this code.
• CW085

  EUDAMED did not publish a description for this code.
• CW106

  EUDAMED did not publish a description for this code.

Primary placement in Germany; available across 2 countries total.

Trade name

not provided

UDI-DI code

34002033006681

Basic UDI-DI

B-34002033006681

Reference / catalog number

900668

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

https://helago-pharma.de/anwendungshinweise/

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.

• D0599OXYGEN PRODUCERS FOR DISINFECTION OF MEDICAL DEVICES - OTHER