FDA UDI In Commercial Distribution 🇺🇸 United States

REF

DI: 00850798007725 · Model: REF-EWCUP-264 · TRANSMED CO, LLC
Product Codes
6
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
REF
Primary DI
00850798007725
Version / Model
REF-EWCUP-264
Company Name
TRANSMED CO, LLC
Labeler DUNS
022637761
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-29
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
d5dc1113-41f8-4edb-9cb9-f884949924c4

Device Description

SMC PRIVATE LABEL Multi-Panel Drug Test Cup, 6 Panel, CLIA Waived, Click Seal Cap, AMP, BZO, COC, mAMP, OPI, THC, 25/BX

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
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
LDJ Enzyme Immunoassay, Cannabinoids
DJG Enzyme Immunoassay, Opiates
LAF Gas Chromatography, Methamphetamine
DJO Indicator, Cellulose Fluorescent, Tlc
JXM Enzyme Immunoassay, Benzodiazepine
DKZ Enzyme Immunoassay, Amphetamine

GMDN Terms

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

Identifiers

Type ID
Package 00850798007749
Package 00850798007732
Primary 00850798007725