Assembly Required Dist., Inc.
Country not established
- Devices
- 1
What Assembly Required Dist., Inc. makes
Assembly Required Dist., Inc. manufactures manual patient transport devices, including universal stretchers (e.g., 1000 Series), specialized rolls (e.g., Rolls 2000), and modular transport systems (e.g., M4 series). These products are designed for intra-facility movement of patients, including stretchers with adjustable features and modular attachments for mobility.
The company’s devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. They are based in the United States and comply with applicable U.S. medical device standards.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Assembly Required Dist., Inc. have in the registry?
The registry currently lists 1 device for Assembly Required Dist., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Assembly Required Dist., Inc.'s devices?
Among its 1 most recently registered device, Assembly Required Dist., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Assembly Required Dist., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Assembly Required Dist., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Assembly Required Dist., Inc. in the registry?
The most recently registered devices listed for Assembly Required Dist., Inc. include UNIVERSAL/1000 SERIES(101S101SDU1100)/ROLLS 2000(2000E)/TRANSPORT(M4).