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Rod Pusher 259-400-230

by RZ-Medizintechnik GmbH GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04049197524520 UDI-DIDate2 May 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Rod Pusher
Generic Name
Rigid endoscopic biopsy forceps, reusable
Model / Reference
259-400-230
Primary DI / UDI-DI
04049197524520
FDA Product Code
HNW
GMDN Term
Rigid endoscopic biopsy forceps, reusable
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Rigid endoscopic biopsy forceps, reusable

Other devices from RZ-Medizintechnik GmbH

See all devices from RZ-Medizintechnik GmbH →

Properties

  • Premarket Exempt
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No