RediTube™ 8040RTUC
RediTube™ 8040RTUC is a Class II device made by Airlife, Inc., cleared under FDA 510(k) K042683 on 18 Feb 2005 and listed in FDA GUDID since 9 Apr 2021 (UDI-DI 10190752152342), active as of 23 Oct 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
1 ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10190752152342 | Date9 Apr 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK042683 | Date18 Feb 2005 | StatusActive |
Official records
- AccessGUDID record 10190752152342
- FDA 510(k) database K042683
Across registries
- FDA 510(k) K042683 decided 18 Feb 2005 Active
- FDA GUDID UDI-DI 10190752152342 listed 9 Apr 2021 Listed
Recalls
-
- Ongoing Z-3172-2026
The 6Fr suction catheter could not pass through the samples smoothly.
Timeline
- Cleared FDA 510(k) K042683
- Listed FDA GUDID 10190752152342
- Recall initiated FDA recalls Z-3172-2026
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- RediTube™
- Generic name
- Basic endotracheal tube, single-use
- Model / Ref / Catalog
- 8040RTUC
- Primary DI / UDI-DI
- 10190752152342
- 510(k) Number
- FDA product code
- BTR
- GMDN term
- Basic endotracheal tube, single-use
- Device class
- Class II
- Regulation number
- 868.5730
- GUDID distribution status
- In Commercial Distribution
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