Puracath Medical, Inc
United StatesFDA applicant, unverified
- Devices
- 7
What Puracath Medical, Inc makes
Puracath Medical, Inc manufactures needleless connectors for intravenous therapy, including the PuraCath Firefly Needleless Connector IT (9005) and a standalone Firefly Needleless Connector. They also produce the Firefly Peritoneal Dialysis Connector Disinfection System, designed for peritoneal dialysis applications.
The company’s products fall under FDA Class II medical devices and are listed via the 510(k) premarket notification process. Puracath Medical, Inc is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
PuraCath Firefly Needleless Connector IT (9005) Ref K251375
Regimes: 510(k) Registry: 510(k)Firefly Needleless Connector Ref K203796
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 963236661
- [email protected]
- Phone
- 6505590388
Frequently asked questions
How many devices does PURACATH MEDICAL, INC have in the registry?
The registry currently lists 7 devices for PURACATH MEDICAL, INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list PURACATH MEDICAL, INC's devices?
Among its 7 most recently registered devices, PURACATH MEDICAL, INC has devices listed in FDA 510(k) (3 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do PURACATH MEDICAL, INC's devices fall under?
Among its 7 most recently registered devices, the classes recorded for PURACATH MEDICAL, INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PURACATH MEDICAL, INC in the registry?
The most recently registered devices listed for PURACATH MEDICAL, INC include Firefly Luer Cover 40401, Firefly UV Disinfection Device 40406, Firefly Transfer Catheter 40398 and Firefly IPA Bottle 40595.