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5027500100

by Stryker Corp.

5027500100 (5027-500-100) is a foot-switch (FDA Class II) made by Stryker Corp., listed in FDA GUDID since 19 Jun 2026 (UDI-DI 07613327631395), 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 Number07613327631395 UDI-DI Date19 Jun 2026ListedStatusListed 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  • Withdrawn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

Generic name
Foot-switch, electrical
Model / Ref / Catalog
5027500100, 5027-500-100
Primary DI / UDI-DI
07613327631395
FDA product code
GWG, EOB
GMDN term
Foot-switch, electrical
Device class
Class II
Regulation number
882.1480, 874.4760
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

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Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)