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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

LFEG01 — Class IIa MDR by Pharmia Oy

MD Atlas
Pharmia Oy

EUDAMED last updated this device on Nov 14, 2025

LFEG01

641795210007CP

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Pharmia Oy
UDI-DI code: 06417952244248
Reference / catalog number: LFEG01

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Manufacturer information

Organization name: Pharmia Oy
SRN: FI-MF-000001469
Manufacturer status: Active

Critical warnings

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

CW999
For use in patients who have an intact oral cavity, ie, no bleeding ulcers.
CW999
Do not use this product in cases where there is no synthesis of saliva or where there are no salivary glands or they are severely damaged.
CW999
Keep out of the reach and sight of children.
CW999
Avoid contact with eyes.
CW999
Do not use the product if the bottle or the spray part is not intact.
CW999
If adverse effects occur or the symptoms worsen during use, stop using the product and consult your doctor.
CW010
EUDAMED did not publish a description for this code.
CW032
Do not use this product after the expiry date.
CW999
Do not use this product if you are hypersensitive to any of the ingredients listed below. In case the product causes an allergic reaction, stop using the product and contact a doctor.
CW999
For adults. Not suitable for children.

Market distribution

Primary placement in Finland; available across 1 country total.

Country	On market since	Until
FinlandPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 06417952244248
Basic UDI-DI: 641795210007CP
Reference / catalog number: LFEG01
Issuing entity: GS1

Classification

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

Device details

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

EMDN nomenclature code(s)

Q0399ENT DEVICES - OTHER

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

Related devices

LDER06641795210001CBOn the market LAMB03B-06417952243968On the market LMED01B-06417952243944On the market LMED07B-06417952244026On the market LMED05B-06417952243975On the market

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.