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LEMM-K9HK, Basic Kit

FDA UDI

Class I (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
LEMM-K9HK, Basic Kit FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
This kit is for law enforcement and civilian K9 providers. The kit focuses on bleeding control and thoracic trauma. FDA UDI
Model / Reference
01459 FDA UDI
Description
This kit is for law enforcement and civilian K9 providers. The kit focuses on bleeding control and thoracic trauma. FDA UDI

Identifiers

Catalog Number
01459 FDA UDI
Primary DI / UDI-DI
00856767008236 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

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

LEMM-K9HK, Basic Kit by Altitude Technologies Inc. — 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

Sources (1)

  • FDA UDI 44aa95d2-82a0-4508-91ad-1d91f3c2550f 35 fields · synced Jun 1, 2026