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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

307138210 — Class I MDR by LUKAS-ERZETT GmbH & Co.KG

MD Atlas
LUKAS-ERZETT GmbH & Co.KG

EUDAMED last updated this device on Apr 29, 2026

307138210

4027497113115WB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LUKAS-ERZETT GmbH & Co.KG
UDI-DI code: 04027497234998
Reference / catalog number: 307138210

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Manufacturer information

Organization name: LUKAS-ERZETT GmbH & Co.KG
SRN: DE-MF-000005344
Manufacturer status: Active

Related devices

3071340014027497113115WBOn the market 356184027497113115WBOn the market A65100102200264027497113115WBOn the market 356034027497113115WBOn the market A2510010224027497113115WBOn the market

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04027497234998
Basic UDI-DI: 4027497113115WB
Reference / catalog number: 307138210
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: 9
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)

V0199CUTTING DEVICES, SINGLE-USE - 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

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.