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Maxcheck

FDA UDI

Class II (US FDA UDI)

by Maxpert Medical LLC.

Identity

Trade Name
MAXCHECK FDA UDI
Generic Name
Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinical FDA UDI
Device Name
12 Panel Rapid Multi-Drug Test Cup FDA UDI
Model / Reference
CDTC121 FDA UDI
Description
12 Panel Rapid Multi-Drug Test Cup FDA UDI

Identifiers

Catalog Number
CDTC121 FDA UDI
Primary DI / UDI-DI
00852359007069 FDA UDI
FDA Product Code
LDJ FDA UDI
LCM FDA UDI
DNK FDA UDI
DJR FDA UDI
DJC FDA UDI
DIO FDA UDI
JXM FDA UDI
DJG FDA UDI
DIS FDA UDI
DKZ FDA UDI
GMDN Term
Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3870 FDA UDI
862.3640 FDA UDI
862.3620 FDA UDI
862.3610 FDA UDI
862.3250 FDA UDI
862.3170 FDA UDI
862.3650 FDA UDI
862.3150 FDA UDI
862.3100 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

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

Maxcheck by Maxpert Medical LLC. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maxpert Medical LLC.

Sources (1)

  • FDA UDI bb67b1e0-bfe3-4e46-a0dc-c02478b56d60 35 fields · synced Jun 8, 2026