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Teecad Vs-V1

by Visura Technologies, LLC

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

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 Number00860226002512 UDI-DI Date6 Jul 2019ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Teecad
Generic Name
Endoscopic video image processing unit
Model / Reference
VS-V1
Primary DI / UDI-DI
00860226002512
510(k) Number
FDA Product Code
ITX, FDS
GMDN Term
Endoscopic video image processing unit
Device Class
Class II
Regulation Number
892.1570, 876.1500
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Cleared under the same submission (K180911)

Other devices from Visura Technologies, LLC

Properties

  • Single Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No