HeltiQ Wond & Oog Spray

Organization name

Aurena Laboratories AB

SRN

SE-MF-000002890

Manufacturer status

Active

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

• CW268

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

  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

  Avoid direct contact between the nozzle and the wound/eye.
• CW999

  Seek medical attention if condition persists or gets worse.
• CW999

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

Primary placement in Netherlands; available across 3 countries total.

Trade name

HeltiQ Wond & Oog Spray

UDI-DI code

07332343300701

Basic UDI-DI

7332343200017D

Reference / catalog number

301458

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

2002-2, Wound and Eye Wash, Isotonic, NaCl, Buffered 100 ml

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.

• M04040101SALINE DRESSINGS, NON-COMBINED