Data from EUDAMED, last updated Jun 12, 2026

Activated Partial Thromboplastin Time Assay Kit(Ellagic Acid)(Coagulation Method)

B-06941377306507

1 reference

IVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk category: IVDD — General
Manufacturer: Shenzhen Dymind Biotechnology Co., Ltd.

Device family identification

Device name: Activated Partial Thromboplastin Time Assay Kit(Ellagic Acid)(Coagulation Method)
Basic UDI-DI: B-06941377306507
Device model: CA-APTT (EA) Specification 3 ：APTT reagent 4.0 mL × 10, CaCl2 solution 4.0 mL × 10
Issuing agency: EUDAMED
Version date: Jun 4, 2026

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk category: IVDD — General
Status: On the market

ReagentProfessional testingAnimal tissues / cells

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

References

1 reference

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Activated Partial Thromboplastin Time Assay Kit(Ellagic Acid)(Coagulation Method)	`NX-0043-02`	`06941377306507`	1	On the market