FDA UDI In Commercial Distribution 🇺🇸 United States

Rapid Response

DI: 00722066003688 · Model: D12.2-1P29-25 · BTNX Inc
Product Codes
10
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Rapid Response
Primary DI
00722066003688
Version / Model
D12.2-1P29-25
Catalog Number
D12.2-1P29-25
Company Name
BTNX Inc
Labeler DUNS
251005005
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-10-25
Public Version
6
Public Version Date
2023-04-20
Public Version Status
Update
Public Device Record Key
9fa9f994-db81-4088-b3b2-1aea7a04fc99

Device Description

Rapid Response Multi Drug Test Panel (Amphetamine, Barbiturate, Buprenorphine, Benzodiazepine, Methamphetamine, Methadone, Opiates, Oxycodone, Phencyclidine, Tricyclic Antidepressant, Cocaine and THC metabolites in urine.

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
LFG Radioimmunoassay, Tricyclic Antidepressant Drugs
LCM Enzyme Immunoassay, Phencyclidine
DIS Enzyme Immunoassay, Barbiturate
JXM Enzyme Immunoassay, Benzodiazepine
LDJ Enzyme Immunoassay, Cannabinoids
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
DJG Enzyme Immunoassay, Opiates
DJR Enzyme Immunoassay, Methadone
DKZ Enzyme Immunoassay, Amphetamine
DJC Thin Layer Chromatography, Methamphetamine

GMDN Terms

Code Name
46994 Multiple drugs of abuse IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Primary 00722066003688
Unit of Use 00722066004074

Premarket Submissions

Submission Number Supplement Number
K121065 000