GUM HYDRAL GEL

Organization name

Sunstar Europe SA

SRN

CH-MF-000023162

Manufacturer status

Active

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

• CW011

  All GUM HYDRAL products are for adults and children 7+ years old under adult supervision
• CW275

  GUM HYDRAL products have not been tested in pregnant or breast-feeding women. If you are taking medicinal products or are pregnant or breast-feeding, ask your doctor or pharmacist for advice before using GUM HYDRAL products
• CW007

  Do not use if the device packaging integrity is damaged
• CW032

  Do not use the device beyond expiry date
• CW129

  Do not use in the presence of hypersensitivity to any ingredients contained in the product
• CW135

  Keep out of reach of children

Primary placement in Spain; available across 25 countries total.

Trade name

GUM HYDRAL GEL

UDI-DI code

17630019900734

Basic UDI-DI

B-17630019900734

Reference / catalog number

6000, 6002

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

GUM HYDRAL GEL is a Class I medical device containing specific ingredients for the management of symptoms of dry mouth and moisturizing the oral cavity for more comfort.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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