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First Responder Kit

FDA UDI

Class I (US FDA UDI)

by Cbx Llc

Identity

Trade Name
First Responder Kit FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
First Responder Kit contains CPR Mask with oxygen port, one pair of nitrile gloves, emergency shears, safety prep razor, dry cleaning towel and NaCl wet wipe. FDA UDI
Model / Reference
FRK101 FDA UDI
Description
First Responder Kit contains CPR Mask with oxygen port, one pair of nitrile gloves, emergency shears, safety prep razor, dry cleaning towel and NaCl wet wipe. FDA UDI

Identifiers

Catalog Number
FRK101 FDA UDI
Primary DI / UDI-DI
B859FRK10109 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

First Responder Kit by Cbx Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cbx Llc

Sources (1)

  • FDA UDI bf4f6696-c5ca-4c0f-88c1-581841d3f50e 34 fields · synced Jun 1, 2026