Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Quick Change Base - Male - Male TI — Class I MDR

MD Atlas
Levitate Technology ApS

EUDAMED last updated this device on Jan 19, 2026

Quick Change Base - Male - Male TI

5715763QCVD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Levitate Technology ApS
UDI-DI code: 05715763006521
Reference / catalog number: LTA100053

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

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: Quick Change Base - Male - Male TI
UDI-DI code: 05715763006521
Basic UDI-DI: 5715763QCVD
Reference / catalog number: LTA100053
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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.