Lucovitaal Keelspray (Hoest) CE 20 ml

Organization name

PK Benelux BV

SRN

NL-MF-000006672

Manufacturer status

Active

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

• CW999

  Warnings: • Keep out of reach of small children; • Stop using in case of hypersensitivity; • Do not use after the expiry date mentioned on the packaging; Use in children only under supervision of an adult • Wash with water if products gets in the eye. Do not use: • If you cannot swallow; • If you are hypersensitive to one of the ingredients; • If younger than 5 years. Use during pregnancy and/or breastfeeding: Cough & Throat Spray is not recommended in pregnant or breastfeeding women due to a lack of adequate available human data on the ingredients of Cough & Throat Spray. Adverse events: The active ingredient Cough & Throat Spray is well tolerated and no serious adverse events have been documented.

Primary placement in Netherlands; available across 1 country total.

Trade name

Lucovitaal Keelspray (Hoest) CE 20 ml

UDI-DI code

D-041018LV

Basic UDI-DI

B-041018LV

Reference / catalog number

041018

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

Symptomatic treatment of sore throat and cough caused by common cold in adults and children older than 5 years

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-041018LV

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

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

• R028099RESPIRATORY CIRCUITS AND MOUNT CATHETERS - ACCESSORIES NOT INCLUDED IN OTHER CLASSES