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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

Blade 10'' AL Kit C3.0 50-60kg — Class I MDR

MD Atlas
Levitate Technology ApS

EUDAMED last updated this device on Jan 16, 2026

Blade 10'' AL Kit C3.0 50-60kg

5715763BladeBP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Levitate Technology ApS
UDI-DI code: 05715763005920
Reference / catalog number: LTA006052

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Manufacturer information

Organization name: Levitate Technology ApS
SRN: DK-MF-000046389
Manufacturer status: Active

Related devices

Adapter Tube 250mm5715763AdapterXDOn the market Blade 10'' AL C2.0 0-40kg5715763BladeBPOn the market Blade 10'' AL C2.5 40-50kg5715763BladeBPOn the market Blade 10'' AL C3.0 50-60kg5715763BladeBPOn the market Blade 10'' AL C3.5 60-70kg5715763BladeBPOn 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 Denmark; available across 1 country total.

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

Device identification

Trade name: Blade 10'' AL Kit C3.0 50-60kg
UDI-DI code: 05715763005920
Basic UDI-DI: 5715763BladeBP
Reference / catalog number: LTA006052
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)

Y062499LOWER EXTREMITY PROSTHESES - 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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