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EUDAMED last updated this device on May 22, 2026
B-697424646LSD000LL28Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Lysergic acid diethylamide(LSD) Rapid Test Kit(Urine) is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by SAFECARE BIOTECH (HANGZHOU) CO., LTD.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
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 →D-697424646LSD000LL28Basic 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 →B-697424646LSD000LL28LSD-1011/LSD-1012/LSD-1014UDI 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 →D-697424646LSD000LL28
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0102160599DRUGS OF ABUSE/TOXICOLOGY RT & POC - OTHERSterile
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 →No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market |
CN-MF-000019109No 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.B-697424646LH001FEGAOn the marketLuteinizing Hormone(LH) Rapid Test Kit (Urine)B-697424646LH000FCFZOn the marketLysergic acid diethylamide(LSD) Rapid Test (Urine)B-697424646LSD001LN2HOn the marketMalaria P.f. Rapid Test (Whole Blood)B-697424646MAL000GKTVOn the marketMalaria P.v. Rapid Test (Whole Blood)B-697424646MAL001GMU6On the marketMalaria P.f. Rapid Test Kit(Whole Blood)B-697424646MAL001GKU2On the market