← Back to catalogue

MasterPeace

FDA UDI

Class I (US FDA UDI)

by Texray AB

Identity

Trade Name
MasterPeace FDA UDI
Generic Name
Patient radiation shielding pad/drape, reusable FDA UDI
Device Name
Versatile Patient Shield to be placed, e.g., over femoralis. Compatible with sterile pouch accessory (not included). FDA UDI
Model / Reference
Versatile Patient Shield FDA UDI
Description
Versatile Patient Shield to be placed, e.g., over femoralis. Compatible with sterile pouch accessory (not included). FDA UDI

Identifiers

Catalog Number
PS3250 FDA UDI
Primary DI / UDI-DI
07350121950498 FDA UDI
FDA Product Code
KPY FDA UDI
GMDN Term
Patient radiation shielding pad/drape, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 30 Centimeter FDA UDI
Length — 60 Centimeter FDA UDI

Category: Patient radiation shielding pad/drape, reusable

MasterPeace by Texray AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient radiation shielding pad/drape, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Texray AB

Sources (1)

  • FDA UDI 2a83ee15-1c9d-4769-9596-f74670dce64c 35 fields · synced May 30, 2026