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Depuy Synthes Evo4K220

by Nds Surgical Imaging, LLC. 3 variants

Listed FDA GUDID listing, not in commercial distribution

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 Number00817613020543 UDI-DI Date8 Nov 2018ListedStatusListed GUDID: not 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  • Withdrawn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
Depuy Synthes
Generic Name
Endoscopic video image processing unit
Model / Reference
Evo4K220
Primary DI / UDI-DI
00817613020543
FDA Product Code
LMB
GMDN Term
Endoscopic video image processing unit
Device Class
Class I
Regulation Number
892.2010
GUDID distribution status
Not in Commercial Distribution

Other devices from Nds Surgical Imaging, LLC.

See all devices from Nds Surgical Imaging, LLC. →

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No