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Legend Aerospace

FDA UDI

Class II (US FDA UDI)

by Legend Aerospace, Inc.

Identity

Trade Name
Legend Aerospace FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Device Name
Enhanced Emergency Medical Kit LAI-5532A1 FDA UDI
Model / Reference
LAI-5532A1 FDA UDI
Description
Enhanced Emergency Medical Kit LAI-5532A1 FDA UDI

Identifiers

Catalog Number
Legend Aerospace Enhanced Emergency Medical Kit LAI-5532A1 FDA UDI
Primary DI / UDI-DI
00850057805017 FDA UDI
FDA Product Code
OKI FDA UDI
GMDN Term
First aid kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: First aid kit, medicated

Legend Aerospace by Legend Aerospace, Inc. — Class II — 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 dd8449e3-f3cb-4d82-a3f4-e0c7e1fd213d 34 fields · synced May 31, 2026