FDA UDI In Commercial Distribution 🇺🇸 United States

ARK™ Fentanyl II Assay

DI: 00812101030561 · Model: 5069-0001-00 · ARK DIAGNOSTICS INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ARK™ Fentanyl II Assay
Primary DI
00812101030561
Version / Model
5069-0001-00
Catalog Number
5069-0001-00
Company Name
ARK DIAGNOSTICS INC
Labeler DUNS
164880598
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-27
Public Version
1
Public Version Date
2020-03-06
Public Version Status
New
Public Device Record Key
d44789cd-0e9e-4cf5-954f-039f725a28cd

Device Description

The ARK™ Fentanyl II Assay is an immunoassay intended for the qualitative determination of fentanyl in human urine at a cutoff concentration of 1.0 ng/mL.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DJG Enzyme Immunoassay, Opiates

GMDN Terms

Code Name
63018 Fentanyl IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 00812101030561

Customer Contacts

Phone
5102706270

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius