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Pro-Tek-To Pad

FDA UDI

Class I (US FDA UDI)

by Flow X-Ray Corp.

Identity

Trade Name
Pro-Tek-To Pad FDA UDI
Generic Name
Patient radiation shielding pad/drape, reusable FDA UDI
Device Name
Pro-Tek-To Pad, Shimmering Electric Blue FDA UDI
Model / Reference
75057-39 FDA UDI
Description
Pro-Tek-To Pad, Shimmering Electric Blue FDA UDI

Identifiers

Primary DI / UDI-DI
00843696129361 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Patient radiation shielding pad/drape, reusable

Pro-Tek-To Pad by Flow X-Ray Corp. — 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

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Manufacturer

Manufacturer
Flow X-Ray Corp.

Sources (1)

  • FDA UDI bb3d5b20-317a-499d-a167-4f470c102792 33 fields · synced Jun 8, 2026