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Vest

FDA UDI

Class I (US FDA UDI)

by Burlington Medical, Llc

Identity

Trade Name
VEST FDA UDI
Generic Name
Radiation shielding apron FDA UDI
Device Name
VESTCE-SEVEST-XSM (CUSTOM: VEST, .35MM ENVIROLITE, XSM) FDA UDI
Model / Reference
SEVESTXSM FDA UDI
Description
VESTCE-SEVEST-XSM (CUSTOM: VEST, .35MM ENVIROLITE, XSM) FDA UDI

Identifiers

Primary DI / UDI-DI
00840186673281 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

Vest 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

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Manufacturer

Sources (1)

  • FDA UDI 8f1a06f8-36ef-4dfd-8fd0-87089a256db4 34 fields · synced Jun 8, 2026