Hangzhou Bever Medical Devices Co., Ltd.
4 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Male, Nelaton-tip Ready-to-Use Hydrophilic Catheter; Femal, Nelaton-tip Ready-to-Use Hydrophilic Catheter; Pediatric, Nelaton-tip Ready-to-Use Hydrophilic Catheter Intermittent Catheter; Male, Tapered-Tip Tiemann Ready-to-Use Hydrophilic Catheter; Male, Olive-Tip Tiemann Ready-to-Use Hydrophilic Catheter (K192468) | Hangzhou Bever Medical Devices Co., Ltd. | 2019-11-27 |
| BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE (K111401) | Hangzhou Bever Medical Devices Co., Ltd. | 2012-07-19 |
| BEVER REINFORCED ENDOTRACHEAL TUBE WITH CUFF (ORAL/NASAL), BEVER REINFORCED ENDOTRACHEAL TUBE WITHOUT CUFF (ORAL/NASAL) (K111406) | Hangzhou Bever Medical Devices Co., Ltd. | 2012-07-19 |
| BEVER UNOCATED / COATED, PAEDIATRIC / MALE / FEMALE NELATON-TIP / TIEMANN-TIP INTERMITTENT CATHETER, (K111405) | Hangzhou Bever Medical Devices Co., Ltd. | 2012-02-13 |
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Every clearance here is in the API, with alerts when new ones post.