- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jun 4, 2026
B-06953825908904U82V, Elektroniczny ciśnienia NARAMIENNY, depan is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Shenzhen Urion Technology Co., Ltd.. Placed on the EU market in Northern Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0695382590890406953825908904(01)06953825908904
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z1203020501NON–INVASIVE OSCILLOMETRIC BLOOD PRESSURE GAUGESCN-MF-000018740G1 078672 0014Primary placement in XI; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| XIPrimary placement | Oct 31, 2024 | Dec 31, 2028 |
| Poland | Oct 31, 2024 | Dec 31, 2028 |
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.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
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 →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.
B-06953825906252On the marketStepcareB-06953825910303On the marketSUNALEB-06953825910310On the marketU82V, Elektroniczny ciśnienia NARAMIENNY, depanB-06953825908898On the marketUpper Arm Electronic Blood Pressure Monitor69538259UABPZJOn the marketUpper Arm Electronic Blood Pressure Monitor69538259UABPZJOn the marketCertificate health across this manufacturer's portfolio.
G10 078672 0022IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
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