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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

20-2492317 Bibs 3 ply 38x68cm — Class I MDR by Ab Fatex Oy

MD Atlas
Ab Fatex Oy

EUDAMED last updated this device on May 6, 2026

20-2492317 Bibs 3 ply 38x68cm

6430072530206Y

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ab Fatex Oy
UDI-DI code: 06430072530053
Reference / catalog number: -

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Manufacturer information

Organization name: Ab Fatex Oy
SRN: FI-MF-000041039
Manufacturer status: Active

Related devices

10-3031347 Protection Sheet 1406430072530106VOn the market 10-3061347 Protection sheet 2106430072530106VOn the market 20-1492360 Bibs 2 ply 38x686430072530206YOn the market -6430072530106VOn the market -6430072530106VOn 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.

Market distribution

Primary placement in Sweden; available across 2 countries total.

Country	On market since	Until
SwedenPrimary placement	Jan 1, 2021	Still on market
Norway	Jan 1, 2021	Still on market

Device identification

Trade name: 20-2492317 Bibs 3 ply 38x68cm
UDI-DI code: 06430072530053
Basic UDI-DI: 6430072530206Y
Reference / catalog number: -
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: 600
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)

T0399PROTECTION DEVICES (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT PPE) - 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

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Expiration date
Manufacturing date
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Software identification