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CN-MF-000032692Measuring Device for Guide Wire is an MDD-legacy medical device registered in EUDAMED. It is classified as Class I. Manufactured by WUHAN MINDRAY SCIENTIFIC CO., LTD.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on May 14, 2026
B-06934635742803Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)06934635742803
1 warning recorded — scroll inside the panel to see all entries.
CW011Sterile
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 Germany; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Sep 30, 2020 | Sep 30, 2070 |
| Austria | Sep 30, 2020 | Sep 30, 2070 |
| Belgium | Sep 30, 2020 | Sep 30, 2070 |
| Bulgaria | Sep 30, 2020 | Sep 30, 2070 |
| Cyprus | Sep 30, 2020 | Sep 30, 2070 |
| Czechia | Sep 30, 2020 | Sep 30, 2070 |
| Denmark | Sep 30, 2020 | Sep 30, 2070 |
| Estonia | Sep 30, 2020 | Sep 30, 2070 |
| EL | Sep 30, 2020 | Sep 30, 2070 |
| Spain | Sep 30, 2020 | Sep 30, 2070 |
| Finland | Sep 30, 2020 | Sep 30, 2070 |
| France | Sep 30, 2020 | Sep 30, 2070 |
| Croatia | Sep 30, 2020 | Sep 30, 2070 |
| Hungary | Sep 30, 2020 | Sep 30, 2070 |
| Ireland | Sep 30, 2020 | Sep 30, 2070 |
| Iceland | Sep 30, 2020 | Sep 30, 2070 |
| Italy | Sep 30, 2020 | Sep 30, 2070 |
| Liechtenstein | Sep 30, 2020 | Sep 30, 2070 |
| Lithuania | Sep 30, 2020 | Sep 30, 2070 |
| Luxembourg | Sep 30, 2020 | Sep 30, 2070 |
| Latvia | Sep 30, 2020 | Sep 30, 2070 |
| Malta | Sep 30, 2020 | Sep 30, 2070 |
| Netherlands | Sep 30, 2020 | Sep 30, 2070 |
| Norway | Sep 30, 2020 | Sep 30, 2070 |
| Poland | Sep 30, 2020 | Sep 30, 2070 |
| Portugal | Sep 30, 2020 | Sep 30, 2070 |
| Romania | Sep 30, 2020 | Sep 30, 2070 |
| Sweden | Sep 30, 2020 | Sep 30, 2070 |
| Slovenia | Sep 30, 2020 | Sep 30, 2070 |
| Slovakia | Sep 30, 2020 | Sep 30, 2070 |
| Türkiye | Sep 30, 2020 | Sep 30, 2070 |
| XI | Sep 30, 2020 | Sep 30, 2070 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
06934635742803Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-06934635742803F16BB-PA00639UDI 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.
L0923ORTHOPAEDICS SURGICAL MEASURERS, REUSABLENo 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.B-06943242365404On the marketMeasuring Device for Guide WireB-06934635734181On the marketMeasuring Device for Guide WireB-06934635742599On the marketMeasuring Device for Guide Wire Φ3.0*250B-06934635742537On the marketMeasuring Device for NailB-06903278124239On the marketMetal Femoral HeadB-06943242304274On the marketNo certificate specifically references this device's Basic UDI-DI.