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Visura TEECAD Carrier CR-P2

by Visura Technologies, LLC

Listed FDA GUDID listing, no authorization on record

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 Number00860226002529 UDI-DI Date26 Jul 2022ListedStatusListed GUDID: 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  • Withdrawn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
Visura TEECAD Carrier
Generic Name
Ultrasound imaging transducer positioning unit
Model / Ref / Catalog
CR-P2, VIS0100
Primary DI / UDI-DI
00860226002529
510(k) Number
FDA Product Code
FDS, ITX
GMDN Term
Ultrasound imaging transducer positioning unit
Device Class
Class II
Regulation Number
876.1500, 892.1570
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Ultrasound imaging transducer positioning unit

Cleared under the same submission (K180911)

Other devices from Visura Technologies, LLC

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

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