Skip to content

S-Scort® 9 2109

by Sscor, Inc.

S-Scort 9 2109, an emergency airway clearance suction system (FDA Class II; FDA product code BTA, Pump, Portable, Aspiration (Manual Or Powered)) made by Sscor, Inc., was listed in FDA GUDID on 13 Feb 2017 (UDI-DI B24521091); the registry lists it as not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 NumberB24521091 UDI-DI Date13 Feb 2017ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
S-Scort® 9
Generic name
Emergency airway clearance suction system, electric
Model / reference
2109
Primary DI / UDI-DI
B24521091
FDA product code
BTA
GMDN term
Emergency airway clearance suction system, electric
Device class
Class II
Regulation number
878.4780
GUDID distribution status
Not in Commercial Distribution

Similar devices

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

Other devices from Sscor, Inc.

See all devices from Sscor, Inc. →

Properties

  • Serial number
Other properties (14, all answered No)