Skip to content

Medical Action Industries 77719D

by Medical Action Industries Inc.

Medical Action Industries 77719D is a Class II device made by Medical Action Industries Inc., listed in FDA GUDID since 29 Oct 2026 (UDI-DI 10809160542255), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10809160542255 UDI-DI Date29 Oct 2026ListedStatusListed 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  • Withdrawn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
Medical Action Industries
Generic name
Vascular access device flush/disinfection tool
Model / reference
77719D
Primary DI / UDI-DI
10809160542255
FDA product code
PEZ
GMDN term
Vascular access device flush/disinfection tool
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution

Other devices from Medical Action Industries Inc.

See all devices from Medical Action Industries Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Combination product
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (7, all answered No)