Skip to content

CIT Ortho 613034702

by Cit Ortho

CIT Ortho 613034702 is a Class II device made by Cit Ortho, listed in FDA GUDID since 23 Apr 2021 (UDI-DI 20850009724063), 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 Number20850009724063 UDI-DI Date23 Apr 2021ListedStatusListed 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  • Withdrawn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
CIT Ortho
Generic name
Rigid optical arthroscope, single-use
Model / reference
613034702
Primary DI / UDI-DI
20850009724063
FDA product code
HRX
GMDN term
Rigid optical arthroscope, single-use
Device class
Class II
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid optical arthroscope, single-use

Similar devices

Other devices filed under FDA product code HRX (Arthroscope).

Other devices from Cit Ortho

See all devices from Cit Ortho →

Properties

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