FDA UDI In Commercial Distribution 🇺🇸 United States

Preview

DI: 00816862022483 · Model: PRE-WDOA-232 · WONDFO USA CO., LTD.
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
Preview
Primary DI
00816862022483
Version / Model
PRE-WDOA-232
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2020-04-24
Public Version
6
Public Version Date
2022-11-14
Public Version Status
Update
Public Device Record Key
f8f34af9-aa8b-4f8e-a8dc-36212b5bb92c

Device Description

3-Panel Preview Dip Card; COC,mAMP,THC

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
LAF Gas Chromatography, Methamphetamine
LDJ Enzyme Immunoassay, Cannabinoids

GMDN Terms

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

Identifiers

Type ID
Package 00816862022506
Primary 00816862022483
Unit of Use 00816862022490

Customer Contacts

Phone
844-337-2743

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius