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Brazos

FDA UDI

Class I (US FDA UDI)

by Dms Holdings, Inc.,

Identity

Trade Name
Brazos FDA UDI
Generic Name
First aid kit, non-medicated, reusable FDA UDI
Device Name
Brazos First Aid Kit - 250pcs FDA UDI
Model / Reference
604-2600-0250 FDA UDI
Description
Brazos First Aid Kit - 250pcs FDA UDI

Identifiers

Primary DI / UDI-DI
00840008019952 FDA UDI
FDA Product Code
OHO FDA UDI
GMDN Term
First aid kit, non-medicated, reusable 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: First aid kit, non-medicated, reusable

Brazos by Dms Holdings, Inc., — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dms Holdings, Inc.,

Sources (1)

  • FDA UDI 5dee0d3b-9f12-458a-a83a-c72c8c8d6b0d 33 fields · synced Jun 8, 2026