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CC-Hook Right 202-1413

by Xiros Ltd 2 variants

CC-Hook Right 202-1413 is a Class I device made by Xiros Ltd, listed in FDA GUDID since 12 Aug 2019 (UDI-DI 05060267131362), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060267131362 UDI-DI Date12 Aug 2019ListedStatusListed 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  • Withdrawn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
CC-Hook Right
Generic name
Suturing unit, single-use
Model / Ref / Catalog
202-1413
Primary DI / UDI-DI
05060267131362
FDA product code
GDG
GMDN term
Suturing unit, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)