SpeediCath Flex Set 28941
SpeediCath Flex Set 28941 is a Class II device made by Coloplast A/S, cleared under FDA 510(k) K222059 on 21 Sep 2022 and listed in FDA GUDID since 5 Feb 2026 (UDI-DI 05708932778114), 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 | Number05708932778114 | Date5 Feb 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK222059 | Date21 Sep 2022 | StatusActive |
Official records
- AccessGUDID record 05708932778114
- FDA 510(k) database K222059
Across registries
- FDA 510(k) K222059 decided 21 Sep 2022 Active
- FDA GUDID UDI-DI 05708932778114 listed 5 Feb 2026 Listed
Timeline
- Cleared FDA 510(k) K222059
- Listed FDA GUDID 05708932778114
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- SpeediCath Flex Set
- Generic name
- Single-administration urethral catheterization kit, single-use
- Model / Ref / Catalog
- 28941
- Primary DI / UDI-DI
- 05708932778114
- 510(k) Number
- FDA product code
- FCM, EZD
- GMDN term
- Single-administration urethral catheterization kit, single-use
- Device class
- Class II
- Regulation number
- 876.5130
- GUDID distribution status
- In Commercial Distribution
- Size
- Catheter Working Length — 13 InchCatheter Gauge — 10 FrenchCatheter Working Length — 33 Centimeter
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