FDA UDI In Commercial Distribution 🇺🇸 United States

SAFElife™

DI: 00816862028249 · Model: CDOA-12135NT · WONDFO USA CO., LTD.
Product Codes
9
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
SAFElife™
Primary DI
00816862028249
Version / Model
CDOA-12135NT
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2026-01-15
Public Version
1
Public Version Date
2026-01-23
Public Version Status
New
Public Device Record Key
6641c55c-8bd0-41c1-a8ce-dd7932e13a19

Device Description

13-Panel T-Cup Compact; AMP1000,BAR300,BUP10,BZO300,COC300,FTY1,MDMA500,MET1000,MOP300,MTD300,OXY100,PCP25,TCA1000

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
NFT Test, Amphetamine, Over The Counter
PTH Test, Barbiturate, 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
QAW Test, Tricyclic Antidepressants, Over The Counter

GMDN Terms

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

Identifiers

Type ID
Unit of Use 00816862028164
Primary 00816862028249

Premarket Submissions

Submission Number Supplement Number
K252550 000