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CrossFlow 0450000000

by Stryker Corp.

CrossFlow 0450000000 is a Class II device made by Stryker Corp., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 07613327058048), 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 Number07613327058048 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  • Withdrawn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

Trade name
CrossFlow
Generic name
Surgical irrigation/aspiration pump, reusable
Model / Ref / Catalog
0450000000
Primary DI / UDI-DI
07613327058048
FDA product code
HRX
GMDN term
Surgical irrigation/aspiration pump, reusable
Device class
Class II
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical irrigation/aspiration pump, reusable

Similar devices in this category

Other devices filed under Surgical irrigation/aspiration pump, reusable.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)