Obesimed Forte 28 c

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: • Do not use Obesimed® Forte in the following situations: - If you are allergic to one or more of the ingredients; - If you have suffered from gastrointestinal disorders; - If you have suffered from esophageal stenosis or pre-existing bowel abnormalities; - When pregnant or breastfeeding. • If you have any doubts about whether you can use Obesimed® Forte and/or can use it in combination with medication, consult your doctor or pharmacist first. • Do not open the capsule before using. • Keep out of reach of small children. Possible side effects: Obesimed® Forte is well tolerated but can lead to a few side effects although not everybody suffers from these side effects. Mild stomach and intestinal complaints may be experienced initially such as thin or loose stools, mild diarrhea, reflux and gas formation or constipation. Usually these side effects disappear after a few days. To avoid these side effects start with a low dosage (1 capsule per meal) and then gradually increase the intake as the body adjusts. If any of these side effects becomes serious, or if you notice any side effects not listed in this instructions for use, consult your doctor or pharmacist. Use during pregnancy and/or breastfeeding: Losing weight is not allowed when pregnant or breastfeeding

Primary placement in Slovenia; available across 1 country total.

Trade name

Obesimed Forte 28 c

UDI-DI code

D-017532MR

Basic UDI-DI

B-017532MR

Reference / catalog number

017532

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 treat obesity and overweight in adults

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-017532MR

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

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

• G0402ORALLY ADMINISTERED DEVICES FOR APPETITE CONTROL AND REDUCTION OF INTESTINAL ABSORPTION