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Zeos 84-24-6431

by Santa Barbara Imaging Systems, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00812231034941 UDI-DI Date19 Jan 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Zeos
Generic Name
Arthroscopic access cannula, single-use
Model / Reference
84-24-6431
Primary DI / UDI-DI
00812231034941
FDA Product Code
NBH
GMDN Term
Arthroscopic access cannula, single-use
Device Class
Class I
Regulation Number
888.1100
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Santa Barbara Imaging Systems, Inc.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

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