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Wolf X-Ray

FDA UDI

Class I (US FDA UDI)

by Flow X-Ray Corp.

Identity

Trade Name
Wolf X-Ray FDA UDI
Generic Name
Radiation shielding apron FDA UDI
Device Name
Front Closing Special Procedure Apron, Medium, Light Weight Lead, Antimicrobial FDA UDI
Model / Reference
68093LW-42 FDA UDI
Description
Front Closing Special Procedure Apron, Medium, Light Weight Lead, Antimicrobial FDA UDI

Identifiers

Primary DI / UDI-DI
00843696148423 FDA UDI
FDA Product Code
EAJ FDA UDI
GMDN Term
Radiation shielding apron 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: Radiation shielding apron

Wolf X-Ray by Flow X-Ray Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation shielding apron.

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 49149b28-d7de-4d1d-b5bb-f5bf9c6803a5 33 fields · synced May 30, 2026