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6000-804-030

by Stryker Leibinger

6000-804-030 (6000-804-032) is a Class II device made by Stryker Leibinger, listed in FDA GUDID since 22 Mar 2023 (UDI-DI 07613327468274), 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 Number07613327468274 UDI-DI Date22 Mar 2023ListedStatusListed 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  • Withdrawn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 planning/navigation-enhancement system
Model / Ref / Catalog
6000-804-030, 6000-804-032
Primary DI / UDI-DI
07613327468274
FDA product code
HAW
GMDN term
Surgical planning/navigation-enhancement system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Unsafe

Related devices

Category: Surgical planning/navigation-enhancement system

Similar devices in this category

Other devices filed under Surgical planning/navigation-enhancement system.

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)