Lucovital D-mannose bruistablet

Organization name

PK Benelux BV

SRN

NL-MF-000006672

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW999

  Warning: • Do not use when allergic to any of the ingredients; • Adverse effects may occur in overdose, such as flatulence, stomach ache or diarrhoea; • Keep out of reach of young children; • If you experience allergic reactions, stop using D-mannose Urinary tract; • The product can cause beeturia (red/pink discoloration of the urine) due to excipient beetroot red extract. Consult your doctor if: • You discover traces of blood in the urine; • Symptoms worsen or persist after 7 days; • You have an existing medical condition or are taking other medication; • You have symptoms of bladder or upper urinary tract infection such as a fever of 38 °C (100.4F) or higher, noncontrollable shivering, nausea (feeling sick), vomiting or diarrhoea. You may suffer from an upper urinary tract infection, which needs additional treatment; • You have a history of kidney stones. Use during pregnancy and/or breastfeeding: No data are available concerning the use of D-mannose Urinary tract during pregnancy or breastfeeding. Therefore you cannot use this product during pregnancy or breastfeeding. Side effect(s): Lucovital® D-Mannose Urinary tract has few side effects and is generally well tolerated. Gastro intestinal symptoms as diarrhea, stomach aches, flatulence are possible side effects.

Primary placement in Netherlands; available across 1 country total.

Trade name

Lucovital D-mannose bruistablet

UDI-DI code

D-081007N4

Basic UDI-DI

B-081007N4

Reference / catalog number

081007

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

To prevent and support the treatment of urinary tract infections

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-081007N4

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

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

• G0499ORALLY ADMINISTERED GASTROINTESTINAL DEVICES - OTHER