Taiwan Armada Enterprise Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 5
What Taiwan Armada Enterprise Co., Ltd. makes
Taiwan Armada Enterprise Co., Ltd. manufactures manual wheelchair models, including the A1000 Super Sport, C650 Series Tour Light, B990K Vivi, A2000 Super Motive, and B900 Super Light. These devices are designed for mobility assistance and vary in features such as weight capacity and frame construction.
The company’s wheelchair portfolio is classified under FDA’s Class I medical devices and is listed via the 510(k) pathway. These products are intended for use in the US market. The manufacturer is based in Taiwan.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Biotech B990K Vivi Wheelchair Ref K014198
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Taiwan Armada Enterprise Co., Ltd. have in the registry?
The registry currently lists 5 devices for Taiwan Armada Enterprise Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Taiwan Armada Enterprise Co., Ltd.'s devices?
Among its 5 most recently registered devices, Taiwan Armada Enterprise Co., Ltd. has devices listed in FDA 510(k) (5 devices).
What risk classes do Taiwan Armada Enterprise Co., Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Taiwan Armada Enterprise Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Taiwan Armada Enterprise Co., Ltd. in the registry?
The most recently registered devices listed for Taiwan Armada Enterprise Co., Ltd. include BIOTECH MANUAL WHEELCHAIR, A1000 SUPER SPORT WHEELCHAIR, BIOTECH MANUAL WHEELCHAIR C650 SERIES TOUR LIGHT WHEELCHAIR, BIOTECH B990K VIVI WHEELCHAIR and BIOTECH MANUAL WHEELCHAIR A2000 SUPER MOTIVE WHEELCHAIR.