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CL22322 Custom Med Label Pack

by Xodus Medical, Inc.

CL22322 Custom Med Label Pack is a Class I device made by Xodus Medical, Inc., listed in FDA GUDID since 8 Dec 2022 (UDI-DI 00787551018509), registry data as of 21 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 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00787551018509 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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
Procedural medication labelling set
Model / Ref / Catalog
CL22322
Primary DI / UDI-DI
00787551018509
FDA product code
LYV
GMDN term
Procedural medication labelling set
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Radiation Sterilization

Related devices

Category: Procedural medication labelling set

Other devices from Xodus Medical, Inc.

See all devices from Xodus Medical, Inc. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (7, all answered No)