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Criti-Kit 200-AI

FDA UDI

Class N (US FDA UDI)

by HF Acquisition Co. LLC

Identity

Trade Name
Criti-Kit 200-AI FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Model / Reference
Criti-Kit 200-AI FDA UDI

Identifiers

Catalog Number
1022670 FDA UDI
Primary DI / UDI-DI
00850065007434 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: First aid kit, medicated

Criti-Kit 200-AI by HF Acquisition Co. LLC — 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 04852f34-6557-4a1f-9d05-57425a2f0131 34 fields · synced May 31, 2026