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Klarity Medical Ez-3200A

by Klarity Medical Products, LLC

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 Number00817355022812 UDI-DI Date24 Mar 2022ListedStatusListed 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  • Withdrawn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
Klarity Medical
Generic Name
Patient positioning thermoplastic mould material
Model / Reference
EZ-3200A
Primary DI / UDI-DI
00817355022812
FDA Product Code
ILH
GMDN Term
Patient positioning thermoplastic mould material
Device Class
Class I
Regulation Number
890.3475
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Related devices

Category: Patient positioning thermoplastic mould material

Other devices from Klarity Medical Products, LLC

See all devices from Klarity Medical Products, LLC →

Properties

  • Lot / Batch Number
  • Expiration Date
  • 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
  • Premarket Exempt: No
  • Serial Number: No