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TACTICAL CricKIT

FDA UDI

Class II (US FDA UDI)

by North American Rescue, Llc.

Identity

Trade Name
TACTICAL CricKIT FDA UDI
Generic Name
Cricothyrotomy kit, single-use FDA UDI
Device Name
KIT, TACTICAL CricKIT - CUSTOM FDA UDI
Model / Reference
85-0291 FDA UDI
Description
KIT, TACTICAL CricKIT - CUSTOM FDA UDI

Identifiers

Catalog Number
85-0291 FDA UDI
Primary DI / UDI-DI
00842209108725 FDA UDI
FDA Product Code
OGP FDA UDI
GMDN Term
Cricothyrotomy kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cricothyrotomy kit, single-use

TACTICAL CricKIT by North American Rescue, Llc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cricothyrotomy kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9a4828d2-2906-40bf-9f97-f17f953dfe4a 34 fields · synced May 30, 2026