Rusch IPN041783
Rusch IPN041783 (120000-000090) is a Class II device made by Teleflex Incorporated, cleared under FDA 510(k) K955564 on 28 Jun 1996 and listed in FDA GUDID since 16 Oct 2015 (UDI-DI 04026704009824), active as of 23 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 | Number04026704009824 | Date16 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK955564 | Date28 Jun 1996 | StatusActive |
Official records
- AccessGUDID record 04026704009824
- FDA 510(k) database K955564
Across registries
- FDA 510(k) K955564 decided 28 Jun 1996 Active
- FDA GUDID UDI-DI 04026704009824 listed 16 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K955564
- Listed FDA GUDID 04026704009824
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Rusch
- Generic name
- Tracheostomy tube, non-reinforced, non-customized, reusable
- Model / Ref / Catalog
- IPN041783, 120000-000090
- Primary DI / UDI-DI
- 04026704009824
- 510(k) Number
- FDA product code
- JOH
- GMDN term
- Tracheostomy tube, non-reinforced, non-customized, reusable
- Device class
- Class II
- Regulation number
- 868.5800
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
- Size
- Lumen/Inner Diameter — 9 MillimeterOuter Diameter — 12.4 Millimeter
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