BrightCare

FDA UDI

Class I (US FDA UDI)

by Firstar Healthcare Company Limited (guangzhou)

Identity

Trade Name: BrightCare FDA UDI
Generic Name: First aid kit, non-medicated, single-use FDA UDI
Device Name: SQ1214 First Aid Kit FDA UDI
Model / Reference: SQ1214 FDA UDI
Description: SQ1214 First Aid Kit FDA UDI

Identifiers

Primary DI / UDI-DI: B448SQ12140 FDA UDI
FDA Product Code: OHO FDA UDI
GMDN Term: First aid kit, non-medicated, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4014 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: First aid kit, non-medicated, single-use

BrightCare by Firstar Healthcare Company Limited (guangzhou) — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Firstar Healthcare Company Limited (guangzhou)

Sources (1)

FDA UDI a93eb0e2-d459-4b03-85ac-af384f73f6db 33 fields · synced May 30, 2026