- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 22, 2026
735010414A200UQXtend Connect Shape A200 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by C LindheXtend AB. Placed on the EU market in Norway. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
SE-MF-000005639No certificate specifically references this device's Basic UDI-DI.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →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.(01)07350104141011
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Norway; available across 9 countries total.
| Country | On market since | Until |
|---|---|---|
| NorwayPrimary placement | — | Still on market |
| Belgium | — | Still on market |
| Germany | — | Still on market |
| Denmark | — | Still on market |
| Finland | — | Still on market |
| France | — | Still on market |
| Italy | — | Still on market |
| Netherlands | — | Still on market |
| Sweden | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
07350104141011Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
735010414A200UQA200-SQFUDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Y062499LOWER EXTREMITY PROSTHESES - OTHER735010414A100UKOn the marketXtend Connect Quick fit unit, Tube clamp 30 mm, Orange735010414A100UKOn the marketXtend Connect Shape A200735010414A200UQOn the marketXtend Foot Först H100, Size 23, Weight max 100 kg, Right Caucasian735010414H100W4On the market735010414H100W4