Set, Administration, Intravascular KMI436
Set, Administration, Intravascular KMI436 is a Class II device made by Mps Medical, Inc, listed in FDA GUDID since 12 Mar 2019 (UDI-DI 00816513023692), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00816513023692 | Date12 Mar 2019 | StatusListed |
Official records
- AccessGUDID record 00816513023692
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Set, Administration, Intravascular
- Generic name
- Medication transfer set
- Model / reference
- KMI436
- Primary DI / UDI-DI
- 00816513023692
- FDA product code
- FPA
- GMDN term
- Medication transfer set
- Device class
- Class II
- Regulation number
- 880.5440
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code FPA (Set, Administration, Intravascular).
- Hospira Administration Sets by Hospira, Inc.
- One Stick Y Extension Set and Volumeter by One Stick, LLC
- Boston Solution Infusion Sets by The Boston Medical Group
- Snapdose Device by Abbott Laboratories
- Sterile Blood Administration Set by Suru Chemicals & Pharmaceuticals, Ltd.
- Miser™ 00884450116982 by Merit Medical Systems, Inc.
- MR Extension Set (001) by University of Michigan
- Energized Drug Container System by Abbott Laboratories
- Solution Set with 1.2 Micron Air Eliminating Filter by Baxter Healthcare Corp
- Merit Medical® 00884450029749 by Merit Medical Systems, Inc.