HANGZHOU BEVER MEDICAL DEVICES CO., LTD.
FDA Regulatory Profile
HANGZHOU BEVER MEDICAL DEVICES CO., LTD. appears in FDA public data with 1 recall, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1061-2026, Class II) was initiated on November 29, 2025. Its most recent 510(k) clearance was granted on November 27, 2019.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-1061-2026 | Class II | BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F | November 29, 2025 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K192468 | Male, Nelaton-tip Ready-to-Use Hydrophilic Catheter; Femal, Nelaton-tip Ready-to-Use Hydrophilic Cat | November 27, 2019 |
| K111406 | BEVER REINFORCED ENDOTRACHEAL TUBE WITH CUFF (ORAL/NASAL), BEVER REINFORCED ENDOTRACHEAL TUBE WITHOU | July 19, 2012 |
| K111401 | BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE | July 19, 2012 |
| K111405 | BEVER UNOCATED / COATED, PAEDIATRIC / MALE / FEMALE NELATON-TIP / TIEMANN-TIP INTERMITTENT CATHETER, | February 13, 2012 |