FDA UDI Not in Commercial Distribution 🇺🇸 United States

ToxCup Drug Screen Cup

DI: 00816555020390 · Model: HT23 · AMEDITECH INC.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ToxCup Drug Screen Cup
Primary DI
00816555020390
Version / Model
HT23
Catalog Number
HT23
Company Name
AMEDITECH INC.
Labeler DUNS
010551716
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-08
Public Version
5
Public Version Date
2023-11-14
Public Version Status
Update
Public Device Record Key
16d8433d-7985-4768-a70c-5a87491506e8
Distribution End Date
2020-04-17

Device Description

ToxCup® Drug Screen Cup (AMP300/COC300/MET500/OPI300/THC50/MDMA500/MTD300)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
DJG Enzyme Immunoassay, Opiates
DJR Enzyme Immunoassay, Methadone
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
DKZ Enzyme Immunoassay, Amphetamine

GMDN Terms

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

Identifiers

Type ID
Primary 00816555020390

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K032057 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
15 – 30 Degrees Celsius