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5450800030

by Stryker Medtech K.K.

5450800030 is a Class I device made by Stryker Medtech K.K., listed in FDA GUDID since 24 Sep 2018 (UDI-DI 07613327291490), 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 Number07613327291490 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  • Withdrawn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
Ultrasonic surgical system torque wrench, reusable
Model / Ref / Catalog
5450800030
Primary DI / UDI-DI
07613327291490
FDA product code
MDM
GMDN term
Ultrasonic surgical system torque wrench, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Ultrasonic surgical system torque wrench, reusable

Other devices from Stryker Medtech K.K.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)