Hangzhou Bever Medical Devices Co., Ltd.
Country not established FDA
- Devices
- 53
- Registrations
- FDA
- FDA recalls
- 11 ongoing
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 devices- Regimes: CE MDR Registry: EUDAMEDGUDID
- Regimes: CE MDR Registry: EUDAMEDGUDID
- Regimes: CE MDR Registry: EUDAMEDGUDID
Showing 51-53 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.
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.
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.