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Air-Flow-Piezon Dw-048A

by E.M.S. Electro Medical Systems S.A. 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

3 ongoing

Recall on shared 510(k) K190124; other models may be affected

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07613353171582 UDI-DI Date13 Jul 2026ListedStatusListed GUDID: in commercial distribution

Recalls

3 recalls · 3 ongoing · FDA

  • 3 recalls, same reason

    • Ongoing Z-1686-2024 FDA Class II initiated 13 Mar 2024 on shared 510(k) K190124
    • Ongoing Z-1687-2024 FDA Class II initiated 13 Mar 2024 on shared 510(k) K190124
    • Ongoing Z-1688-2024 FDA Class II initiated 13 Mar 2024 on shared 510(k) K190124

    Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Air-Flow-Piezon
Generic Name
Electromechanical device/system transport trolley
Model / Ref / Catalog
DW-048A
Primary DI / UDI-DI
07613353171582
510(k) Number
FDA Product Code
EJR
GMDN Term
Electromechanical device/system transport trolley
Device Class
Class I
Regulation Number
872.6030
GUDID distribution status
In Commercial Distribution

Other devices from Electro Medical Systems (Ems Sa)

See all devices from Electro Medical Systems (Ems Sa) →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No