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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

Reinforcement-Arm — Class I MDR by medical bees GmbH

MD Atlas
medical bees GmbH

EUDAMED last updated this device on Sep 18, 2024

Reinforcement-Arm

042515541TD0303STATIKUNHE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: medical bees GmbH
UDI-DI code: 04251554151502
Reference / catalog number: MB2-20-402-00

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Manufacturer information

Organization name: medical bees GmbH
SRN: DE-MF-000005814
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: Reinforcement-Arm
UDI-DI code: 04251554151502
Basic UDI-DI: 042515541TD0303STATIKUNHE
Reference / catalog number: MB2-20-402-00
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L0318INSTRUMENTS FOR SUPPORT OF SURGICAL DEVICES, 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

This device is not currently linked to any other device.

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.