Shandong Qiaopai Group Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Shandong Qiaopai Group Co., Ltd. makes
Shandong Qiaopai Group Co., Ltd. manufactures sterile hypodermic needles and scalp vein sets, including the Model TW SB and Model TW LB. These products are designed for single-use intravenous access and subcutaneous injections in clinical settings.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Shandong Qiaopai Group Co., Ltd. have in the registry?
The registry currently lists 1 device for Shandong Qiaopai Group Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shandong Qiaopai Group Co., Ltd.'s devices?
Among its 1 most recently registered device, Shandong Qiaopai Group Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Shandong Qiaopai Group Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Shandong Qiaopai Group Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shandong Qiaopai Group Co., Ltd. in the registry?
The most recently registered devices listed for Shandong Qiaopai Group Co., Ltd. include MODEL TW SB, SCALP VEIN SET; MODEL TW LB, STERILE HYPODERMIC NEEDLE.