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Immunalysis

FDA UDI

Class I (US FDA UDI)

by Immunalysis Corporation

Identity

Trade Name
Immunalysis FDA UDI
Generic Name
Cannabinoid/cannabinoid metabolite IVD, control FDA UDI
Device Name
cTHC Urine Control Set FDA UDI
Model / Reference
3005-5 FDA UDI
Description
cTHC Urine Control Set FDA UDI

Identifiers

Catalog Number
3005-5 FDA UDI
Primary DI / UDI-DI
00840937108383 FDA UDI
FDA Product Code
LAS FDA UDI
GMDN Term
Cannabinoid/cannabinoid metabolite IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.3280 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

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

No

FDA UDI

Category: Cannabinoid/cannabinoid metabolite IVD, control

Immunalysis by Immunalysis Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cannabinoid/cannabinoid metabolite IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 06134126-4d06-4f3c-8f2b-ea43184aac52 35 fields · synced May 30, 2026