FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00841824103962 · Model: W22104 · W.H.P.M. INC.
Product Codes
8
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
N/A
Primary DI
00841824103962
Version / Model
W22104
Company Name
W.H.P.M. INC.
Labeler DUNS
602085672
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2018-06-06
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
1f5de47d-322c-4390-8671-d8e7edcfe1c7

Device Description

DOA 10 in 1 Test Dip Card, 25Pcs/Box, CLIA Waived BARB/BUP/BZO/COC/mAMP/MTD/OPI/OXY/TCA/THC

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
LFG Radioimmunoassay, Tricyclic Antidepressant Drugs
DJG Enzyme Immunoassay, Opiates
DJR Enzyme Immunoassay, Methadone
LAF Gas Chromatography, Methamphetamine
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
JXM Enzyme Immunoassay, Benzodiazepine
DIS Enzyme Immunoassay, Barbiturate

GMDN Terms

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

Identifiers

Type ID
Primary 00841824103962
Unit of Use 00841824103979