Hangzhou Bever Medical Devices Co., Ltd.
Country not established FDA
- Devices
- 53
- Registrations
- FDA
- FDA recalls
- 11 ongoing
At a glance
Market reach
- United States
- FDA establishment, FDA recalls
What Hangzhou Bever Medical Devices Co., Ltd. makes
The company manufactures single-administration urethral drainage catheters designed for intermittent urinary catheterization, including models like the BD Intermittent.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 53 devicesShowing 1-50 of 53
Company details
- DUNS number
- 528185295
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 1
- 2026 0
2025
- 29 Nov 2025 Z-1061-2026 Class II Ongoing Labeling error, Incorrect expiration date
FDA establishments
- Hangzhou Bever Medical Devices Co., Ltd. Hangzhou Zhejiang · CN FEI 3008729910
Frequently asked questions
How many devices does Hangzhou Bever Medical Devices Co., Ltd. have in the registry?
The registry currently lists 53 devices for Hangzhou Bever Medical Devices Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hangzhou Bever Medical Devices Co., Ltd.'s devices?
Among its 50 most recently registered devices, Hangzhou Bever Medical Devices Co., Ltd. has devices listed in EUDAMED (21 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Hangzhou Bever Medical Devices Co., Ltd.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Hangzhou Bever Medical Devices Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Hangzhou Bever Medical Devices Co., Ltd.?
FDA recall records list 1 recall initiated by Hangzhou Bever Medical Devices Co., Ltd., the most recent initiated on 29 Nov 2025. 1 of them is recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Hangzhou Bever Medical Devices Co., Ltd. in the registry?
The most recently registered devices listed for Hangzhou Bever Medical Devices Co., Ltd. include Intermittent Catheter 010024, Intermittent Catheter 010026, Intermittent Catheter 010025 and Intermittent Catheter 010028.
Which FDA establishments are linked to Hangzhou Bever Medical Devices Co., Ltd.?
1 FDA establishment is linked to Hangzhou Bever Medical Devices Co., Ltd. in the registry; they are listed on the company page.