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Adventure Medical Kits

FDA UDI

Class N (US FDA UDI)

by Adventure Ready Brands

Identity

Trade Name
Adventure Medical Kits FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Device Name
Sportsman 300 FDA UDI
Model / Reference
1 FDA UDI
Description
Sportsman 300 FDA UDI

Identifiers

Catalog Number
0105-0300 FDA UDI
Primary DI / UDI-DI
00707708303005 FDA UDI
FDA Product Code
LRR FDA UDI
GMDN Term
First aid kit, medicated FDA UDI

Classification

Device Class
N 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

Yes

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

Yes

FDA UDI

Category: First aid kit, medicated

Adventure Medical Kits by Adventure Ready Brands — 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 434e13ef-ea1b-49bd-a76d-58880eb8e7c5 35 fields · synced Jun 8, 2026