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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

91120699 — Class I MDR by CEFLA s.c.

MD Atlas
CEFLA s.c.

EUDAMED last updated this device on Oct 15, 2025

91120699

803383793TRSUCTIO10013T

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CEFLA s.c.
UDI-DI code: 08033837932956
Reference / catalog number: 91120699

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View device family (Basic UDI)

Manufacturer information

Organization name: CEFLA s.c.
SRN: IT-MF-000009228
Manufacturer status: Active

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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.

Critical warnings

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

CW018
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08033837932956
Basic UDI-DI: 803383793TRSUCTIO10013T
Reference / catalog number: 91120699
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: Device to be used in dental practice which, connected to the suction line of the dental unit, allows suction of water, air, body fluids of oral and nasal origin. Suitable to be used also as dental dam stretcher support. For a better effectiveness of the device, position the suction mouth in the quadrant of question; the suction mouth can be positioned on the lower or upper arch, right or left quadrants.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08033837932956

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Q019001SALIVA ASPIRATORS AND SALIVA ABSORBENTS

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

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