FDA UDI In Commercial Distribution 🇺🇸 United States

iScreen™

DI: 00817405023325 · Model: ABTDUAW17702B · Instant Technologies, Inc.
Product Codes
6
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
iScreen™
Primary DI
00817405023325
Version / Model
ABTDUAW17702B
Catalog Number
ABTDUAW17702B
Company Name
Instant Technologies, Inc.
Labeler DUNS
019410187
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2022-11-09
Public Version
1
Public Version Date
2022-11-17
Public Version Status
New
Public Device Record Key
f25f268c-9aaf-4476-a449-1bca2d8d7682

Device Description

7 PANEL CLIA WAIVED SQUARE CUP AMP1000, BZO300, COC300, MET1000, MOP300, OXY100, THC50 SVT (CR,OX,S.G.)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
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
NFY Test, Cocaine And Cocaine Metabolites, Over The Counter
NFT Test, Amphetamine, Over The Counter
NFV Test, Benzodiazepine, Over The Counter
NGG Test, Methamphetamine, 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 30817405023326
Primary 00817405023325
Unit of Use 10817405023322

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius