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EUDAMED last updated this device on May 21, 2026
B-697424646THC000KUZ4Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Marijuana(THC) 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-697424646THC000KUZ4Basic 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-697424646THC000KUZ4THC-1011/THC-1012/THC-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 →D-697424646THC000KUZ4
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0102160505CANNABINOIDS - RT & POCSterile
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-697424646HP000FQHZOn the market"Human Chorionic Gonadotropin(HCG) Rapid Test Kit(Urine/Serum)"B-697424646HCG002E9NZOn the market6-Monoacetylmorphine(6-MAM) Rapid TestB-6974246466-MAM000D3X6On the market6-Monoacetylmorphine(6-MAM) Rapid Test(Saliva)B-6974246466-MAM002D7XQOn the market6-Monoacetylmorphine(6-MAM) Rapid Test(Urine)B-6974246466-MAM001D5XFOn the market