Martech Medical Products
Country not established FDA establishment FEI 2527072
- Devices
- 11
- Registrations
- FDA
- FDA recalls
- 0
What Martech Medical Products makes
Martech Medical Products manufactures introducer sheaths, including PTFE-coated super sheath introducers and coaxial introducer sets. These devices are designed for vascular access procedures, facilitating catheter insertion and stabilization within blood vessels.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) pathway. These devices are intended for use in the United States.
Catalogue
Search and filter all 11 devicesCompany details
- FDA FEI number
- 2527072
- Address
- 1500 DELP DR., HARLEYSVILLE, PA, 19438
Frequently asked questions
How many devices does MARTECH MEDICAL PRODUCTS have in the registry?
The registry currently lists 11 devices for MARTECH MEDICAL PRODUCTS. Devices recorded under merged duplicate company entries are counted once.
Which registries list MARTECH MEDICAL PRODUCTS's devices?
Among its 11 most recently registered devices, MARTECH MEDICAL PRODUCTS has devices listed in FDA 510(k) (11 devices).
What risk classes do MARTECH MEDICAL PRODUCTS's devices fall under?
Among its 11 most recently registered devices, the classes recorded for MARTECH MEDICAL PRODUCTS's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from MARTECH MEDICAL PRODUCTS in the registry?
The most recently registered devices listed for MARTECH MEDICAL PRODUCTS include 25G Huber Needle, NEOLINE(TM), PTFE SUPER SHEATH INTRODUCER and NEEDLE GUARD(TM).