EKHP00310

Organization name

Ekuberg Pharma

SRN

IT-MF-000010732

Manufacturer status

Active

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

• CW007

  EUDAMED did not publish a description for this code.
• CW135

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

  Close the tube properly with the cap after using the product. Wash the cannula after each use. Keep out of reach of children. Do not use on damaged skin and mucous membranes. Do not swallow. Do not use in case of hypersensitivity or allergy to one of the ingredients. Do not use after the expiry date indicated at the bottom of the package and on the tube.
• CW999

  No side effects and contraindications are known under normal and reasonably foreseeable use described in this package insert. In the light of current scientific knowledge, there is no known evidence to exclude the use of the product in pregnant women.

Primary placement in Italy; available across 3 countries total.

Trade name

not provided

UDI-DI code

D-EKHP0031025

Basic UDI-DI

B-EKHP0031025

Reference / catalog number

EKHP00310

Issuing entity

EUDAMED

Risk category

Class IIa

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

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

D-EKHP0031025

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

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

• M9002PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)