FDA UDI In Commercial Distribution 🇺🇸 United States

QuickProfile™ Oxycodone Test Card

DI: M90107RD71010 · Model: 07RD7101 · LUMIQUICK DIAGNOSTICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
QuickProfile™ Oxycodone Test Card
Primary DI
M90107RD71010
Version / Model
07RD7101
Catalog Number
07RD7101
Company Name
LUMIQUICK DIAGNOSTICS, INC.
Labeler DUNS
790175165
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-15
Public Version
7
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
46873f04-60bd-433e-8430-3dd87b4470f8

Device Description

Immunoassay for the detection of oxycodone in human urine

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
46994 Multiple drugs of abuse IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Package M90107RD71011
Primary M90107RD71010
Package M90107RD71012

Customer Contacts

Device Sizes

Type Value Unit Text
Length 75 Millimeter

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
4 – 30 Degrees Celsius