- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Sep 15, 2023
B-06973094411400Cervix Brush.Cervical Cell Sampler is an MDD-legacy medical device registered in EUDAMED. It is classified as Class I. Manufactured by Junocare Medical Devices Ltd. Placed on the EU market in Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
CN-MF-000030653(01)06973094411400
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 EL; available across 8 countries total.
| Country | On market since | Until |
|---|---|---|
| ELPrimary placement | — | Still on market |
| Austria | — | Still on market |
| Belgium | — | Still on market |
| Denmark | — | Still on market |
| France | — | Still on market |
| Italy | — | Still on market |
| Netherlands | — | Still on market |
| Türkiye | — | 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.
06973094411400Basic 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-06973094411400CGJS1JN18UDI 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.
U089002DEVICES FOR GYNAECOLOGICAL CYTOLOGYPrimary 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.
697309441vails10CBOn the marketCell Preservative Fluid697309441vails10CBOn the marketCervix Brush697309441CB10795On the marketCervix Brush.Cervical Cell Sampler697309441Brush**V3On the marketCervix Brush.Cervical Cell Sampler697309441Brush**V3On the marketCervix Brush.Cervical Cell Sampler697309441Brush**V3On the marketNo 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.