Sims Deltec, Inc.
United StatesFDA applicant, unverified
- Devices
- 32
What Sims Deltec, Inc. makes
Sims Deltec, Inc. manufactures implantable venous access systems, including low-profile ports like the PORT-A-CATH and its trans-arterial percutaneous variant, as well as peripherally inserted catheters such as the CLINICATH IR and POLYFLOW series. The company also produces administration sets for medication delivery, including flexible reservoirs (e.g., CADD 250ML), filtered sets (e.g., 0.2µ and 1.2µ bacterial filters), and anti-siphon valve systems. Needle de-access enclosures (e.g., SIMS SILO) and specialized components like the CADD CHECKVALVE administration set are part of its portfolio.
These devices are classified under FDA Class II and are authorised via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) registry. Sims Deltec, Inc. is headquartered in the United States.
Catalogue
Search and filter all 32 devicesFrequently asked questions
How many devices does Sims Deltec, Inc. have in the registry?
The registry currently lists 32 devices for Sims Deltec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sims Deltec, Inc.'s devices?
Among its 32 most recently registered devices, Sims Deltec, Inc. has devices listed in FDA 510(k) (32 devices).
What risk classes do Sims Deltec, Inc.'s devices fall under?
Among its 32 most recently registered devices, the classes recorded for Sims Deltec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sims Deltec, Inc. in the registry?
The most recently registered devices listed for Sims Deltec, Inc. include PORT-A-CATH P.A.S. PORT II IMPLANTABLE VENOUS ACCESS SYTEMS, SIMS SILO NEEDLE DE-ACCESS ENCLOSURE, PORT-A-CATH II TRANS-ARTERIAL PERCUTANEOUS SYSTEM and CADD ADMINISTRATION SET, CADD 250ML FLEXIBLE MEDICATION RESERVOIR, MODIFIED SECURIT SHELL, SECURITY SHELL ADAPTER.