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FS EZ IO Kit Manual 6PK

FDA UDI

Class II (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
FS EZ IO Kit Manual 6PK FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
This EZ-IO kit comes with 6 Field Stripped (FS) manual infusion sets, individually packaged for TRAINING USE ONLY and is NOT intended for human use. FDA UDI
Model / Reference
021171 FDA UDI
Description
This EZ-IO kit comes with 6 Field Stripped (FS) manual infusion sets, individually packaged for TRAINING USE ONLY and is NOT intended for human use. FDA UDI

Identifiers

Primary DI / UDI-DI
00856767008106 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
First aid kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

FS EZ IO Kit Manual 6PK by Altitude Technologies Inc. — Class II — 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 33cbffde-9e92-4b7a-a8b7-a0c809450388 33 fields · synced May 30, 2026