Prestigepro 6421
Prestigepro 6421 is a Class I device made by Prestige Ameritech, listed in FDA GUDID since 4 Apr 2025 (UDI-DI 00840490800021), registry data as of 23 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 | Number00840490800021 | Date4 Apr 2025 | StatusListed |
Official records
- AccessGUDID record 00840490800021
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Prestigepro
- Generic name
- Venous tourniquet, single-use
- Model / Ref / Catalog
- 6421
- Primary DI / UDI-DI
- 00840490800021
- FDA product code
- GAX
- GMDN term
- Venous tourniquet, single-use
- Device class
- Class I
- Regulation number
- 878.5900
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code GAX (Tourniquet, Nonpneumatic).
- Tender and Tiny Tourniquets 11TH by Small Beginnings, Inc.
- CONPHAR VELCRO TOUNIGUER by Conphar, Inc.
- TOURNEQUET, NON-PNEUMATIC by Hemox, Inc.
- TMT (Tactical Mechanical Tourniquet) - US PDF185 by SAFEGUARD MEDICAL TECHNOLOGIES LIMITED
- PRESSURE-QUET TOURNIQUET by Nutec Med, Inc.
- Tourni-Cot - Medium TCM by Mar-Med Co.
- VELCRO TOURNIQUET by Cp Medical
- DISPOSIQUET A DISPOS. TOURNIQUET by Med Lab Products
- LATEX PENROSE DRAIN TUBING by Abco Dealers, Inc.
- UNIVERSAL TOURNIQUET by Dryden Corp.