- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jun 10, 2026
697052264SJPOX0001UKConcentrated Cleaning Fluid is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Sichuan Orienter Biotechnology Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0697052264836010 mL/tube×10CN-MF-000003026(01)06970522648360
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.
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.
Primary placement in Germany; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
| Spain | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0580IVD GENERAL USE CONSUMABLES DEVICES - OTHER ACCESSORIESPrimary 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 →IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
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-06970522646380On the marketChemiluminescence Reaction Vessel697052264YQ11KJOn the marketConcentrated Cleaning Fluid697052264SJPOX0001UKOn the marketCytokeratin 19 Fragment (CYFRA21-1) Assay Kit (Chemiluminescent Immunoassay)B-06970522641941On the marketD-Dimer (D-D) Assay Kit (Chemiluminescent Immunoassay)B-06942028501647On the marketDaily Maintenance Solution697052264SJMYX0004X8On 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.