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MasterPeace Versatile Patient Shield

by Texray AB 4 variants

MasterPeace Versatile Patient Shield (PS3250) is a Class I device made by Texray AB, listed in FDA GUDID since 25 Feb 2025 (UDI-DI 07350121950504), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07350121950504 UDI-DI Date25 Feb 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
MasterPeace
Generic name
Patient radiation shielding pad/drape, reusable
Model / Ref / Catalog
Versatile Patient Shield, PS3250
Primary DI / UDI-DI
07350121950504
FDA product code
KPY
GMDN term
Patient radiation shielding pad/drape, reusable
Device class
Class I
Regulation number
892.6500
GUDID distribution status
In Commercial Distribution
Size
Width — 30 Centimeter
Length — 90 Centimeter

Related devices

Category: Patient radiation shielding pad/drape, reusable

Similar devices

Other devices filed under FDA product code KPY (Shield, Protective, Personnel).

Other devices from Texray AB

See all devices from Texray AB →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)