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Certified Drug Free Urine

FDA UDI

Class I (US FDA UDI)

by Utak Laboratories, Inc.

Identity

Trade Name
CERTIFIED DRUG FREE URINE FDA UDI
Generic Name
Multiple urine analyte IVD, control FDA UDI
Device Name
CERTIFIED DRUG FREE URINE FDA UDI
Model / Reference
CDF U 1L SMA FDA UDI
Description
CERTIFIED DRUG FREE URINE FDA UDI

Identifiers

Catalog Number
CDF U 1L SMA FDA UDI
Primary DI / UDI-DI
B800CDFU1LSMA0 FDA UDI
FDA Product Code
LAS FDA UDI
GMDN Term
Multiple urine analyte 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

No

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

Dimensions & Sizes

Size
Total Volume — 1000 Microliter FDA UDI

Category: Multiple urine analyte IVD, control

Certified Drug Free Urine by Utak Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple urine analyte IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d808ef5e-8bf9-439c-ae4d-b0a8f2227687 37 fields · synced May 30, 2026