SureCath 28032
SureCath 28032 is a Class II device made by Coloplast A/S, cleared under FDA 510(k) K973070 on 6 Nov 1997 and listed in FDA GUDID since 2 Sep 2016 (UDI-DI 05708932021371), active (FDA 510(k)), not in commercial distribution (GUDID) 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 | Number05708932021371 | Date2 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK973070 | Date6 Nov 1997 | StatusActive |
Official records
- AccessGUDID record 05708932021371
- FDA 510(k) database K973070
Across registries
- FDA 510(k) K973070 decided 6 Nov 1997 Active
- FDA GUDID UDI-DI 05708932021371 listed 2 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K973070
- Listed FDA GUDID 05708932021371
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- SureCath
- Generic name
- Single-administration urethral catheterization kit, single-use
- Model / Ref / Catalog
- 28032
- Primary DI / UDI-DI
- 05708932021371
- 510(k) Number
- FDA product code
- EZD
- GMDN term
- Single-administration urethral catheterization kit, single-use
- Device class
- Class II
- Regulation number
- 876.5130
- GUDID distribution status
- Not in Commercial Distribution
- Size
- Total Volume — 700 MilliliterOuter Diameter — 4.7 MillimeterLength — 40 CentimeterCatheter Gauge — 14 French
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