Golden Bridge International, Inc.
Country not established
- Devices
- 1
What Golden Bridge International, Inc. makes
Golden Bridge International, Inc. manufactures the GBI TSH Neonatal Screening Kit, a diagnostic device used to measure thyroid-stimulating hormone (TSH) levels in newborns to detect congenital hypothyroidism.
The company’s portfolio is regulated under FDA’s Class II device classification, with the GBI TSH Neonatal Screening Kit listed via a 510(k) clearance. The company is based in the United States.
Catalogue
Gbi Tsh Neonatal Screening Kit Ref K072458
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Golden Bridge International, Inc. have in the registry?
The registry currently lists 1 device for Golden Bridge International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Golden Bridge International, Inc.'s devices?
Among its 1 most recently registered device, Golden Bridge International, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Golden Bridge International, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Golden Bridge International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Golden Bridge International, Inc. in the registry?
The most recently registered devices listed for Golden Bridge International, Inc. include GBI TSH NEONATAL SCREENING KIT.