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TheraTouch SW1 SW1000

by Drive Devilbiss Healthcare United States GUDID

Product code ISA

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00092237626764 UDI-DIDate27 Mar 2025ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 23 Oct 2026)

Specification

GUDID · synced 23 Oct 2026

Trade Name
TheraTouch SW1
Generic Name
Multidisciplinary extracorporeal shock wave therapy system, mobile
Model / Reference
SW1000
Primary DI / UDI-DI
00092237626764
FDA Product Code
ISA
GMDN Term
Multidisciplinary extracorporeal shock wave therapy system, mobile
Device Class
Class I
Regulation Number
890.5660
Commercial Distribution
In Commercial Distribution

Related devices

Category: Multidisciplinary extracorporeal shock wave therapy system

Other devices from Drive Devilbiss Healthcare

See all devices from Drive Devilbiss Healthcare →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • FDA UDI ec711aaa-8a18-42d0-bb16-b5bd90e703ee 34 fields · synced 23 Oct 2026