AuST Steerable Sheath ADS-MD-002962
AuST Steerable Sheath ADS-MD-002962 is a vascular guide-catheter (FDA Class II) made by CenterPoint Systems LLC, cleared under FDA 510(k) K260942 on 7 Apr 2026 and listed in FDA GUDID since 6 Aug 2026 (UDI-DI 00810024672608), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00810024672608 | Date6 Aug 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK260942 | Date7 Apr 2026 | StatusActive |
Official records
- AccessGUDID record 00810024672608
- FDA 510(k) database K260942
Across registries
- FDA 510(k) K260942 decided 7 Apr 2026 Active
- FDA GUDID UDI-DI 00810024672608 listed 6 Aug 2026 Listed
Timeline
- Cleared FDA 510(k) K260942
- Listed FDA GUDID 00810024672608
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- AuST Steerable Sheath
- Generic name
- Vascular guide-catheter, single-use
- Model / reference
- ADS-MD-002962
- Primary DI / UDI-DI
- 00810024672608
- 510(k) Number
- FDA product code
- DYB, DRA
- GMDN term
- Vascular guide-catheter, single-use
- Device class
- Class II
- Regulation number
- 870.1340, 870.1280
- GUDID distribution status
- In Commercial Distribution
- Size
- Catheter Working Length — 74 Centimeter
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