FDA UDI In Commercial Distribution 🇺🇸 United States

Rapid Response Multi-Drug Integrated Split Spec. Cup

DI: 10722066005290 · Model: D10.3-1K · BTNX Inc
Product Codes
9
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Rapid Response Multi-Drug Integrated Split Spec. Cup
Primary DI
10722066005290
Version / Model
D10.3-1K
Company Name
BTNX Inc
Labeler DUNS
251005005
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2023-04-28
Public Version
1
Public Version Date
2023-05-08
Public Version Status
New
Public Device Record Key
f49abd54-48ba-4350-8696-6805b36dfc4b

Device Description

Multi-Drug Integrated Split Spec. Cup (D10.3-1K) - COC300 AMP1000 MET1000 THC50 OPI2000 PCP25 BAR300 BZO300 MTD300 MDMA500.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
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
Yes
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
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
DJG Enzyme Immunoassay, Opiates
DJR Enzyme Immunoassay, Methadone
DIS Enzyme Immunoassay, Barbiturate
JXM Enzyme Immunoassay, Benzodiazepine
DJC Thin Layer Chromatography, Methamphetamine
LCM Enzyme Immunoassay, Phencyclidine
LDJ Enzyme Immunoassay, Cannabinoids

GMDN Terms

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

Identifiers

Type ID
Unit of Use 00722066005293
Primary 10722066005290