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Drager L049-700-010

by Allied Medical LLC

Drager L049-700-010 is a Class II device made by Allied Medical LLC, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00026072011355), 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 Number00026072011355 UDI-DI Date16 Sep 2016ListedStatusListed 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  • Withdrawn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
Drager
Generic name
General-purpose surgical suction system, vacuum
Model / Ref / Catalog
L049-700-010
Primary DI / UDI-DI
00026072011355
FDA product code
BTA
GMDN term
General-purpose surgical suction system, vacuum
Device class
Class II
Regulation number
878.4780
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose surgical suction system, vacuum

Similar devices

Other devices filed under FDA product code BTA (Pump, Portable, Aspiration (Manual Or Powered)).

Other devices from Allied Medical LLC

See all devices from Allied Medical LLC →

Properties

  • Prescription use
  • Premarket exempt
  • Manufacturing date
Other properties (12, all answered No)