Data from EUDAMED, last updated Jun 11, 2026

InfluenzaA+B&COVID-19 (SARS-CoV-2)Antigen Test Kit（Colloidal Gold）

69520627J017LD

5 references

IVDR Class C

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class C
Manufacturer: ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD

Device family identification

Device name: InfluenzaA+B&COVID-19 (SARS-CoV-2)Antigen Test Kit（Colloidal Gold）
Basic UDI-DI: 69520627J017LD
Device model: Cassette
Issuing agency: GS1
Version date: May 30, 2025

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class C
Status: On the market

Self-testingAnimal tissues / cells

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

References

5 references

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Influenza A+B & COVID-19 (SARS-CoV-2) Antigen Test Kit (Colloidal Gold)	`COVAg+FluAB1NST-3`	`06952062710752`	3	On the market
Influenza A+B & COVID-19 (SARS-CoV-2) Antigen Test Kit (Colloidal Gold)	`COVAg+FluAB1NST-15`	`06952062710776`	15	On the market
Influenza A+B & COVID-19 (SARS-CoV-2) Antigen Test Kit (Colloidal Gold)	`COVAg+FluAB1NST-1`	`06952062710707`	1	On the market
Influenza A+B & COVID-19 (SARS-CoV-2) Antigen Test Kit (Colloidal Gold)	`COVAg+FluAB1NST-20`	`06952062710783`	20	On the market
Influenza A+B & COVID-19 (SARS-CoV-2) Antigen Test Kit (Colloidal Gold)	`COVAg+FluAB1NST-2`	`06952062710745`	2	On the market