| Brand Name | Bivona Tubes Adult Aire-Cuf |
| Common Device Name | Tube Tracheostomy and Tube Cuff |
| Manufacturer (Section D) |
| ICU Medical Healthcare Manufacturing S.A. de C.V. |
| avenida calidad no.4, parque |
| industrial international |
| tijuana NA 22425 |
| MX 22425 |
|
| Manufacturer Contact |
|
reed
covert
|
| 6000 nathan lane north, |
| minneapolis, MN 55442
|
|
+1(224)706-2300
|
|
| MDR Report Key | 50024964 |
| Report Number | 3012307300-2026-07706 |
| Device Sequence Number | 21225638 |
| Product Code |
JOH
|
| UDI-Device Identifier | 15021312006421 |
| Combination Product (Y/N) | N |
| Initial Reporter State | NA |
| Initial Reporter Country | FR |
| PMA/510(K) Number | K083641 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Foreign,Health Professional,User Facility |
| Initial Reporter Occupation |
Pharmacist
|
| Type of Report
| Initial |
| Report Date (Section B) |
07/24/2026 |
| 1 Device was Involved in the Event |
|
| 1 Patient was Involved in the Event |
|
| Is this an Adverse Event Report? |
No
|
| Is this a Product Problem Report? |
Yes
|
| Operator of Device |
Other
|
| Device Catalogue Number | 750180 |
| Device Lot Number | 4201737 |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
Yes
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 07/03/2026 |
| Initial Report FDA Received Date | 07/27/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| Is the Device Labeled for Single Use? (Y/N) |
Yes
|
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Usage of Device |
Initial
|
| Patient Sequence Number | 1 |
| Patient Sex | Unknown |
| Patient Weight | 213 LB |
|
|