- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 12, 2025
697135542U05PAUltrasonic Diagnostic System is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Shenzhen Wisonic Medical Technology Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06971355420222Piloter ExpCN-MF-000005656(01)06971355420222
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning recorded — scroll inside the panel to see all entries.
The Ultrasonic Diagnostic System is prohibited for ophthalmic use or any possible ways that cause the acoustic beam to pass through the eye.
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 Germany; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Feb 28, 2025 | Nov 5, 2028 |
| Spain | Feb 28, 2025 | Nov 5, 2028 |
| Italy | Feb 28, 2025 | Nov 5, 2028 |
| Poland | Feb 28, 2025 | Nov 5, 2028 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z11040104MULTIDISCIPLINARY ULTRASOUND SCANNERS (INTERNAL AND CARDIOLOGY, ETC.)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 →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →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 certificate specifically references this device's Basic UDI-DI.
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.697135542U02P4On the marketUltrasonic Diagnostic System697135542U06PCOn the marketUltrasonic Diagnostic System697135542U05PAOn the marketUltrasonic Diagnostic System697135542U05PAOn the marketUltrasonic Diagnostic System697135542U03P6On the marketUltrasonic Diagnostic System697135542U05PAOn the market