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Genomadix Cube CYP2C19

FDA UDI

Class II (US FDA UDI)

by Genomadix, Inc.

Identity

Trade Name
Genomadix Cube CYP2C19 FDA UDI
Generic Name
Nucleic acid amplification mastermix kit IVD FDA UDI
Device Name
Each unit is a box of 5 training kits (containing water). FDA UDI
Model / Reference
2 FDA UDI
Description
Each unit is a box of 5 training kits (containing water). FDA UDI

Identifiers

Primary DI / UDI-DI
G257ASM001160 FDA UDI
510(k) Number
K220026 FDA UDI
FDA Product Code
NTI FDA UDI
GMDN Term
Nucleic acid amplification mastermix kit IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3360 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nucleic acid amplification mastermix kit IVD

Genomadix Cube CYP2C19 by Genomadix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid amplification mastermix kit IVD.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Genomadix, Inc.

Sources (1)

  • FDA UDI c889c82f-0410-45bf-be13-e48878a59a1a 35 fields · synced May 30, 2026