TruWave 50P172
by Becton, Dickinson and Company
Listed
Valid until
Not applicable
FDA recalls
1 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00885403527398 | Date29 Aug 2026 | StatusListed |
Recalls
-
- Ongoing Z-0413-2024
Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- TruWave
- Generic Name
- Invasive blood pressure monitoring tubing set
- Model / Ref / Catalog
- 50P172
- Primary DI / UDI-DI
- 00885403527398
- 510(k) Number
- FDA Product Code
- DXO
- GMDN Term
- Invasive blood pressure monitoring tubing set
- Device Class
- Class II
- Regulation Number
- 870.2870
- GUDID distribution status
- In Commercial Distribution
- MRI Safety
- MR Safe
- Size
- Length — 180 Centimeter
Other devices from Becton, Dickinson and Company
Properties
Other properties (8)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No