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5920000202

by Stryker Corp.

5920000202 (5920-000-202) is a Class I device made by Stryker Corp., listed in FDA GUDID since 24 Sep 2018 (UDI-DI 07613154599103), 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 Number07613154599103 UDI-DI Date24 Sep 2018ListedStatusListed 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  • Withdrawn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
Surgical pneumatic tourniquet system
Model / Ref / Catalog
5920000202, 5920-000-202
Primary DI / UDI-DI
07613154599103
FDA product code
KCY
GMDN term
Surgical pneumatic tourniquet system
Device class
Class I
Regulation number
878.5910
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 10.0 Feet

Related devices

Category: Surgical pneumatic tourniquet system

Similar devices in this category

Other devices filed under Surgical pneumatic tourniquet system.

Other devices from Stryker Corp.

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Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)