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Prestigepro 6420

by Prestige Ameritech

Prestigepro 6420 is a Class I device made by Prestige Ameritech, listed in FDA GUDID since 4 Apr 2025 (UDI-DI 00840490800014), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840490800014 UDI-DI Date4 Apr 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Prestigepro
Generic name
Venous tourniquet, single-use
Model / Ref / Catalog
6420
Primary DI / UDI-DI
00840490800014
FDA product code
GAX
GMDN term
Venous tourniquet, single-use
Device class
Class I
Regulation number
878.5900
GUDID distribution status
In Commercial Distribution

Related devices

Category: Venous tourniquet, single-use

Similar devices

Other devices filed under FDA product code GAX (Tourniquet, Nonpneumatic).

Other devices from Prestige Ameritech

See all devices from Prestige Ameritech →

Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)