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Customed 152570148312

by Customed, Inc.

Customed 152570148312 (CUS12) is a Class II device made by Customed, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI M208CUS120), 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 NumberM208CUS120 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: 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  • Withdrawn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
Customed
Generic name
Airway suction catheter
Model / Ref / Catalog
152570148312, CUS12
Primary DI / UDI-DI
M208CUS120
FDA product code
JOL
GMDN term
Airway suction catheter
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Airway suction catheter

Other devices from Customed, Inc.

See all devices from Customed, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)