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0207058000

by Stryker Corp.

0207058000 is a Class II device made by Stryker Corp., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04546540184696), 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 Number04546540184696 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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 irrigation system nozzle
Model / Ref / Catalog
0207058000
Primary DI / UDI-DI
04546540184696
FDA product code
FQH
GMDN term
Surgical irrigation system nozzle
Device class
Class II
Regulation number
880.5475
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical irrigation system nozzle

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)