Data from EUDAMED, last updated Jun 12, 2026

Human Metapneumovirus (hMPV) Test Kit

697241261IHMP-502TL

5 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: Human Metapneumovirus (hMPV) Test Kit
Basic UDI-DI: 697241261IHMP-502TL
Device model: IHMP-502-01;IHMP-502-05; IHMP-502-20; IHMP-502-25; IHMP-502-40
Issuing agency: GS1
Version date: Jun 4, 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.

References

5 references

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
LYHER	`IHMP-502-05`	`06972412615902`	1	On the market
LYHER	`IHMP-502-40`	`06972412617722`	1	On the market
LYHER	`IHMP-502-20`	`06972412615339`	1	On the market
LYHER	`IHMP-502-01`	`06972412618279`	1	On the market
LYHER	`IHMP-502-25`	`06972412611737`	1	On the market