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OxyArm™ OA-DA-3025

by Southmedic Incorporated

OxyArm™ OA-DA-3025 is a Class I device made by Southmedic Incorporated, listed in FDA GUDID since 18 Dec 2020 (UDI-DI 10620974000041), 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 Number10620974000041 UDI-DI Date18 Dec 2020ListedStatusListed 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  • Withdrawn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
OxyArm™
Generic name
Vortex oxygen face mask
Model / Ref / Catalog
OA-DA-3025
Primary DI / UDI-DI
10620974000041
FDA product code
CAT
GMDN term
Vortex oxygen face mask
Device class
Class I
Regulation number
868.5340
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vortex oxygen face mask

Similar devices

Also classified as Vortex oxygen face mask.

Other devices from Southmedic Incorporated

See all devices from Southmedic Incorporated →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)