FDA UDI In Commercial Distribution 🇺🇸 United States

T-Dip

DI: 00816862023039 · Model: WDOA-334 · WONDFO USA CO., LTD.
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
T-Dip
Primary DI
00816862023039
Version / Model
WDOA-334
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2023-08-03
Public Version
1
Public Version Date
2023-08-11
Public Version Status
New
Public Device Record Key
c2ed2b14-41f7-4708-99a4-843aaed8697d

Device Description

3-Panel Card;COC300,OPI2000,THC50

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
NFY Test, Cocaine And Cocaine Metabolites, Over The Counter
NGL Test, Opiates, 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
Package 10816862023036
Primary 00816862023039
Unit of Use 00816862023183

Customer Contacts

Phone
630-468-2199

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius