FDA UDI In Commercial Distribution 🇺🇸 United States

ARK™ Ketamine Assay (115mL)

DI: 00812101030011 · Model: 5056-0001-01 · ARK DIAGNOSTICS INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ARK™ Ketamine Assay (115mL)
Primary DI
00812101030011
Version / Model
5056-0001-01
Catalog Number
5056-0001-01
Company Name
ARK DIAGNOSTICS INC
Labeler DUNS
164880598
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-23
Public Version
1
Public Version Date
2019-07-31
Public Version Status
New
Public Device Record Key
cb7060d4-81d3-45b4-9301-bd66b47631a7

Device Description

The ARK™ Ketamine Assay is intended for the qualitative and semiquantitative determination of ketamines in human urine at a cutoff concentration of 50 ng/mL. The assay provides a simple and rapid analytical screening procedure for detecting ketamines in urine and is designated for professional use on automated clinical chemistry analyzers.

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
DKZ Enzyme Immunoassay, Amphetamine

GMDN Terms

Code Name
62129 Ketamine/ketamine metabolite IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 00812101030011

Customer Contacts

Phone
5102706270

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius