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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

2110033 — Class IIa MDR by Ernst Kratz GmbH

MD Atlas
Ernst Kratz GmbH

EUDAMED last updated this device on May 9, 2022

2110033

425560862000AC

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ernst Kratz GmbH
UDI-DI code: 14255608600012
Reference / catalog number: 2110033

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Manufacturer information

Organization name: Ernst Kratz GmbH
SRN: DE-MF-000012746
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	May 9, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 14255608600012
Basic UDI-DI: 425560862000AC
Reference / catalog number: 2110033
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: 12
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)

L0202SUTURE NEEDLES, REUSABLE

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

211003320425560861000A5On the market 14020204425560863000AKOn the market 2010033425560862000ACOn 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.