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OxyArm™ OA-DA-2025

by Southmedic Incorporated

OxyArm™ OA-DA-2025 is a Class II device made by Southmedic Incorporated, listed in FDA GUDID since 1 Sep 2016 (UDI-DI 10620974000034), 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 Number10620974000034 UDI-DI Date1 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Breathing circuit gas-sampling/monitoring set
Model / Ref / Catalog
OA-DA-2025
Primary DI / UDI-DI
10620974000034
FDA product code
CCK
GMDN term
Breathing circuit gas-sampling/monitoring set
Device class
Class II
Regulation number
868.1400
GUDID distribution status
Not in Commercial Distribution

Other devices from Southmedic Incorporated

See all devices from Southmedic Incorporated →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)