Ally® Adhesive Remover

Organization name

Aurena Laboratories AB

SRN

SE-MF-000002890

Manufacturer status

Active

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

• CW054

  EUDAMED did not publish a description for this code.
• CW268

  EUDAMED did not publish a description for this code.
• CW157

  EUDAMED did not publish a description for this code.
• CW140

  EUDAMED did not publish a description for this code.
• CW139

  EUDAMED did not publish a description for this code.
• CW999

  Do not expose to temperatures exceeding 50°C/122°F.
• CW999

  Protect from sunlight.
• CW999

  Keep out of reach of children.
• CW999

  Do not use in confined spaces.
• CW999

  Use only as directed.
• CW999

  Do not spray on sensitive areas of skin (eyes, mouth, ears, nose and vagina).
• CW999

  Stop using if irritation due to dryness of skin occurs, contact healthcare professionals for help if conditions persist or get worse.
• CW999

  If any serious incident occurs in relation to the device, report to the local competent authority and the manufacturer.

Primary placement in Austria; available across 20 countries total.

Trade name

Ally® Adhesive Remover

UDI-DI code

07332343300350

Basic UDI-DI

7332343200157Q

Reference / catalog number

301414

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

REF 2005-1, Adhesive Remover 50 ml

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

• M9003SOLUTIONS FOR ADHESIVE TAPE REMOVAL