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DeVilbiss 7305D-633

by DeVilbiss Healthcare LLC.

DeVilbiss 7305D-633 is a Class II device made by DeVilbiss Healthcare LLC., listed in FDA GUDID since 10 Mar 2017 (UDI-DI 00885304000662), 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 Number00885304000662 UDI-DI Date10 Mar 2017ListedStatusListed 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  • Withdrawn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
DeVilbiss
Generic name
Surgical suction system collection container, single-use
Model / Ref / Catalog
7305D-633
Primary DI / UDI-DI
00885304000662
FDA product code
KDQ
GMDN term
Surgical suction system collection container, single-use
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical suction system collection container, single-use

Similar devices in this category

Other devices filed under Surgical suction system collection container, single-use.

Other devices from DeVilbiss Healthcare LLC.

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Properties

  • Premarket exempt
Other properties (14, all answered No)