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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

DBL 000522-1 — Class I MDR by Websinger Gesellschaft…

MD Atlas
Websinger Gesellschaft m.b.H.

EUDAMED last updated this device on May 20, 2026

DBL 000522-1

912004021CD01U5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Websinger Gesellschaft m.b.H.
UDI-DI code: 09120040210533
Reference / catalog number: DBL 000522-1

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Manufacturer information

Organization name: Websinger Gesellschaft m.b.H.
SRN: AT-MF-000024865
Manufacturer status: Active

Related devices

DBL 160503-U912004021CD01U5On the market DBL 030115912004021CD01U5On the market DBL 050812-U912004021CD01U5On the market 005217 LL912004021CD01U5On the market DBL 030116-1912004021CD01U5On 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 Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Czechia		Still on market

Device identification

Trade name: not provided
UDI-DI code: 09120040210533
Basic UDI-DI: 912004021CD01U5
Reference / catalog number: DBL 000522-1
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: 600 x 1000 mm/200 mm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T030102COVER SHEATHS, INSTRUMENTS AND EQUIPMENTS

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
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Software identification