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BrightCare

FDA UDI

Class N (US FDA UDI)

by The Gilbert Group Llc

Identity

Trade Name
BrightCare FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Model / Reference
SQ1210 FDA UDI

Identifiers

Primary DI / UDI-DI
00856614007764 FDA UDI
FDA Product Code
LRR FDA UDI
OHO FDA UDI
GMDN Term
First aid kit, medicated FDA UDI

Classification

Device Class
N FDA UDI
Regulation Number
878.4014 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: First aid kit, medicated

BrightCare by The Gilbert Group Llc — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fddb70ae-1c43-4274-bee6-63f7401977b3 32 fields · synced May 30, 2026