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EUDAMED last updated this device on Apr 21, 2026
0845357001062WE[01062K] KWIK-STIK™ E. coli O126:K71(B16):H2 NCTC 8622 is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class B. Manufactured by Microbiologics, INC.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
30845357032776[01062K] KWIK-STIK™ E. coli O126:K71(B16):H2 NCTC 8622(01)30845357032776
European Medical Device Nomenclature — the EU product classification assigned to this device.
W01040601QC STRAINS BACTERIOLOGY1 warning recorded — scroll inside the panel to see all entries.
CW011US-MF-000000466No 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.The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | — | Still on market |
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 →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 →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 →08453570023199On the market[0867K] KWIK-STIK™ V. parvula ATCC 10790™084535700867AUOn the market[0697K] KWIK-STIK™ R. equi ATCC 6939™084535700697ATOn the market[0817L] LYFO DISK™ S. Abaetetuba ATCC 35640™084535700817ADOn the market[0260K] KWIK-STIK™ A. psychrolactophilus ATCC 700733™0845357002609GOn the market[0436P] KWIK-STIK™ S. agalactiae (B) ATCC 27956™0845357004369VOn the marketNo certificate specifically references this device's Basic UDI-DI.