FDA UDI In Commercial Distribution 🇺🇸 United States

Preview

DI: 00816862021189 · Model: PRE-PDOA-7125 · WONDFO USA CO., LTD.
Product Codes
10
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
Preview
Primary DI
00816862021189
Version / Model
PRE-PDOA-7125
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2018-06-13
Public Version
6
Public Version Date
2022-11-14
Public Version Status
Update
Public Device Record Key
d5fbca85-3b92-47d0-a325-c6dc8a5cc3c8

Device Description

12-Panel Preview Cup; AMP,BAR,BZO,COC,MDMA,MET,MOP,MTD,OXY,PCP,TCA,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
LDJ Enzyme Immunoassay, Cannabinoids
LFG Radioimmunoassay, Tricyclic Antidepressant Drugs
LCM Enzyme Immunoassay, Phencyclidine
DJR Enzyme Immunoassay, Methadone
DJG Enzyme Immunoassay, Opiates
LAF Gas Chromatography, Methamphetamine
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
JXM Enzyme Immunoassay, Benzodiazepine
DIS Enzyme Immunoassay, Barbiturate
DKZ Enzyme Immunoassay, Amphetamine

GMDN Terms

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

Identifiers

Type ID
Package 10816862021186
Primary 00816862021189
Unit of Use 00816862028188

Customer Contacts

Phone
844-337-2743

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius