← Back to catalogue

F111

FDA UDI

Class I (US FDA UDI)

by Burlington Medical, Llc

Identity

Trade Name
F111 FDA UDI
Generic Name
Radiation shielding apron FDA UDI
Device Name
RPRF111-8XF (F111: 1 Piece Wrap Around with Wide Stretch Belt .5MM PRESTIGE, 8XF) FDA UDI
Model / Reference
RPRF111-8XF FDA UDI
Description
RPRF111-8XF (F111: 1 Piece Wrap Around with Wide Stretch Belt .5MM PRESTIGE, 8XF) FDA UDI

Identifiers

Primary DI / UDI-DI
00840331206517 FDA UDI
FDA Product Code
IWO 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiation shielding apron

F111 by Burlington Medical, Llc — 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

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

Manufacturer

Sources (1)

  • FDA UDI 4dba55e9-b26d-4688-82e0-f696fc6f1716 33 fields · synced May 30, 2026