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PRO1TEK 2+ Patient IFAK Kit

FDA UDI

Class I (US FDA UDI)

by Pro1tek

Identity

Trade Name
PRO1TEK 2+ Patient IFAK Kit FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Device Name
PRO1TEK 2+ Patient IFAK Kit with Wound Spray, Bleeding Control tools with Hemostatic Dressing and other Trauma Kit First-Aid Equipment. FDA UDI
Model / Reference
B283E1BB0 FDA UDI
Description
PRO1TEK 2+ Patient IFAK Kit with Wound Spray, Bleeding Control tools with Hemostatic Dressing and other Trauma Kit First-Aid Equipment. FDA UDI

Identifiers

Primary DI / UDI-DI
B283E1BB0 FDA UDI
FDA Product Code
OVR FDA UDI
GMDN Term
First aid kit, medicated 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: First aid kit, medicated

PRO1TEK 2+ Patient IFAK Kit by Pro1tek — Class I — 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

Manufacturer
Pro1tek

Sources (1)

  • FDA UDI 469f4913-10ed-4f03-bf21-249432df595d 33 fields · synced May 30, 2026