Data from EUDAMED, last updated Jun 11, 2026

Respiratory multiple 7 in 1 test kit (FluA/FluB/COVID-19/RSV/Adeno/MP/HMPV)

0697241261IRS-572BQ

2 references

IVDR Class B

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class B
Manufacturer: Hangzhou Laihe Biotech Co., Ltd.

Data from EUDAMED, last updated Jun 11, 2026

0697241261IRS-572BQ

2 references

IVDR Class B

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class B
Manufacturer: Hangzhou Laihe Biotech Co., Ltd.

Device family identification

Device name: Respiratory multiple 7 in 1 test kit (FluA/FluB/COVID-19/RSV/Adeno/MP/HMPV)
Basic UDI-DI: 0697241261IRS-572BQ
Device model: 303041901
Issuing agency: GS1
Version date: Jan 27, 2026

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

ReagentProfessional testingAnimal tissues / cells

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

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
LYHER	`IRS-572`	`06972412614721`	1	On the market
LYHER	`303041901`	`06972412613823`	1	On the market

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
LYHER	`IRS-572`	`06972412614721`	1	On the market
LYHER	`303041901`	`06972412613823`	1	On the market