Gilford
Country not established
- Devices
- 10
What Gilford makes
Gilford manufactures immunology reagents, including immunoglobulin M, G, and A reagents, complement C3 and C4 reagents, and EIA rubella tests, along with assay controls and a data management system.
The company's products are listed in the FDA 510(k) registry and include both Class I and Class II devices. Gilford is based in the US.
Catalogue
Gilford Immunoglobulin M Reagent Ref K853469
Regimes: 510(k) Registry: 510(k)Eia Rubella Ref K812787
Regimes: 510(k) Registry: 510(k)Advantage Ref K840120
Regimes: 510(k) Registry: 510(k)Gilford Tri-Level Assayed Immunology Control Ref K851202
Regimes: 510(k) Registry: 510(k)Impact 400 #1447X2 Ref K833067
Regimes: 510(k) Registry: 510(k)Gilford Immunoglobulin G Reagent Ref K853465
Regimes: 510(k) Registry: 510(k)Gilford C4 Complement Reagent Ref K853468
Regimes: 510(k) Registry: 510(k)Gilford C3 Complement Reagent Ref K853466
Regimes: 510(k) Registry: 510(k)Data Mgmt. System Ref K842500
Regimes: 510(k) Registry: 510(k)Gilford Immunoglobulin A Reagent Ref K853467
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gilford have in the registry?
The registry currently lists 10 devices for Gilford. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gilford's devices?
Among its 10 most recently registered devices, Gilford has devices listed in FDA 510(k) (10 devices).
What risk classes do Gilford's devices fall under?
Among its 10 most recently registered devices, the classes recorded for Gilford's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gilford in the registry?
The most recently registered devices listed for Gilford include GILFORD IMMUNOGLOBULIN M REAGENT, EIA RUBELLA, ADVANTAGE and GILFORD TRI-LEVEL ASSAYED IMMUNOLOGY CONTROL.