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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

F0140PSE — Class I MDR by Fittydent International…

MD Atlas
Fittydent International GmbH

EUDAMED last updated this device on May 12, 2026

F0140PSE

9002240HKPD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Fittydent International GmbH
UDI-DI code: 09002240000056
Reference / catalog number: F0140PSE

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Manufacturer information

Organization name: Fittydent International GmbH
SRN: AT-MF-000016986
Manufacturer status: Active

Critical warnings

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

CW999
Do not use fittydent Denture Adhesive with other adhesive products. Do not use on dentures with soft lining. Keep out of reach of children. Do not use in case of intolerance/hypersensitivity to any of the ingredients. Do not use on diseased oral mucosa.

Market distribution

Primary placement in Sweden; available across 3 countries total.

Country	On market since	Until
SwedenPrimary placement		Still on market
Denmark		Still on market
Norway		Still on market

Device identification

Trade name: not provided
UDI-DI code: 09002240000056
Basic UDI-DI: 9002240HKPD
Reference / catalog number: F0140PSE
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Denture Adhesive for dentures only
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010280PROSTHETIC DENTISTRY DEVICES - ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.