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N/A 74030

by Stryker Sustainability Solutions

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

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 Number07613327500226 UDI-DI Date18 Jul 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Bed/chair occupant movement pressure/vibration sensor
Model / Ref / Catalog
74030
Primary DI / UDI-DI
07613327500226
FDA Product Code
KMI
GMDN Term
Bed/chair occupant movement pressure/vibration sensor
Device Class
Class I
Regulation Number
880.2400
GUDID distribution status
In Commercial Distribution
Size
Length — 8.0 Feet

Related devices

Category: Bed/chair occupant movement pressure/vibration sensor

Other devices from Stryker Sustainability Solutions

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Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No