FDA UDI In Commercial Distribution 🇺🇸 United States

PRIME SCREEN®

DI: 00810174470987 · Model: DTDOA-1144-10BX-A · WONDFO USA CO., LTD.
Product Codes
11
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
PRIME SCREEN®
Primary DI
00810174470987
Version / Model
DTDOA-1144-10BX-A
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2025-12-05
Public Version
1
Public Version Date
2025-12-15
Public Version Status
New
Public Device Record Key
062205e6-ff0a-42b1-9dc9-a82e2eb73076

Device Description

14-Panel T-Cup 10 per Box; AMP,BAR,BUP,BZO,CO C,MET,MDMA,MTD,OPI,OXY,PCP,PPX,TCA,THC

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
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
PTH Test, Barbiturate, Over The Counter
NFT Test, Amphetamine, Over The Counter
NGL Test, Opiates, Over The Counter
NFV Test, Benzodiazepine, Over The Counter
NFY Test, Cocaine And Cocaine Metabolites, Over The Counter
NGG Test, Methamphetamine, Over The Counter
PTG Test, Methadone, Over The Counter
LCM Enzyme Immunoassay, Phencyclidine
QBF Test, Propoxyphene, Over The Counter
QAW Test, Tricyclic Antidepressants, Over The Counter
NFW Test, Cannabinoid, Over The Counter

GMDN Terms

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

Identifiers

Type ID
Unit of Use 00810174470970
Primary 00810174470987

Customer Contacts

Phone
630-468-2199

Premarket Submissions

Submission Number Supplement Number
K182701 000