Hangzhou Bever Medical Devices Co., Ltd.
Hangzhou Bever Medical Devices Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2019, with 1 FDA device recall on record.
Top product codes for Hangzhou Bever Medical Devices Co., Ltd.
FDA recalls by Hangzhou Bever Medical Devices Co., Ltd.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Hangzhou Bever Medical Devices Co., Ltd.
- K192468 — Male, Nelaton-tip Ready-to-Use Hydrophilic Catheter +4 more
- K111401 — BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE
- K111406 — BEVER REINFORCED ENDOTRACHEAL TUBE WITH CUFF (ORAL/NASAL), BEVER REINFORCED ENDOTRACHEAL TUBE WITHOUT CUFF (ORAL/NASAL)
- K111405 — BEVER UNOCATED / COATED, PAEDIATRIC / MALE / FEMALE NELATON-TIP / TIEMANN-TIP INTERMITTENT CATHETER,
Data sourced from openFDA. This site is unofficial and independent of the FDA.