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Blocker

FDA UDI

Class I (US FDA UDI)

by Burlington Medical, Llc

Identity

Trade Name
BLOCKER FDA UDI
Generic Name
Radiation shielding apron FDA UDI
Device Name
BLOCKER SET - Standard Size with Hook and Loop Closure, .25mm Xenolite 800 NL Size S8T, 12"L X 14"W, 14"L X 16"W, 16"L X 18"W FDA UDI
Model / Reference
U8BLOCKERSET FDA UDI
Description
BLOCKER SET - Standard Size with Hook and Loop Closure, .25mm Xenolite 800 NL Size S8T, 12"L X 14"W, 14"L X 16"W, 16"L X 18"W FDA UDI

Identifiers

Primary DI / UDI-DI
00840331273069 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

Blocker 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 e9fd5bca-eeaa-470f-9586-4c99f46a30fb 33 fields · synced May 30, 2026