FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040186746 · Model: 5703928 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Henry Schein
Primary DI
10304040186746
Version / Model
5703928
Catalog Number
5703928
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2024-12-10
Public Version
1
Public Version Date
2024-12-18
Public Version Status
New
Public Device Record Key
4cb62ef2-3b3e-416c-aeb6-9a39a0de6635

Device Description

14 panel urine drug screen, AMP1000, BAR300, BUP10, BZO300, COC300, EDDP300, mAMP/MET1000, MDMA500, MOP300, MTD300, OXY100, PCP25, TCA1000, 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
Yes
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

GMDN Terms

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

Identifiers

Type ID
Unit of Use 00304040186749
Primary 10304040186746