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Fluid Trap MGVSFT10

by Megadyne Medical Products, Inc.

Fluid Trap MGVSFT10 is a Class II device made by Megadyne Medical Products, Inc., listed in FDA GUDID since 5 Sep 2018 (UDI-DI 10614559104477), 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 Number10614559104477 UDI-DI Date5 Sep 2018ListedStatusListed 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  • Withdrawn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
Fluid Trap
Generic name
Surgical plume evacuation system filter
Model / Ref / Catalog
MGVSFT10
Primary DI / UDI-DI
10614559104477
FDA product code
GAZ
GMDN term
Surgical plume evacuation system filter
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GAZ (Tubing, Noninvasive).

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  • Megadyne 0012A

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See all devices from Megadyne Medical Products, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)