Data from EUDAMED, last updated Jun 11, 2026

iFlash-Rubella IgG

692591270105GY

2 references

IVDR Class C

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

Device family identification

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

ReagentProfessional testingHuman tissues / cellsAnimal tissues / cells

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

References

2 references

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
iFlash-Rubella IgG	`C88035G-S`	`06925912723639`	1	On the market
iFlash-Rubella IgG	`C88035G-L`	`06925912715672`	1	On the market