FDA UDI In Commercial Distribution 🇺🇸 United States

reditest®

DI: 10858904006522 · Model: 011020190 · REDWOOD TOXICOLOGY LABORATORY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
reditest®
Primary DI
10858904006522
Version / Model
011020190
Catalog Number
DMA-U114
Company Name
REDWOOD TOXICOLOGY LABORATORY, INC.
Labeler DUNS
929599280
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-09-24
Public Version
6
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
6225e7e5-09ae-458c-b801-a74dc280d449

Device Description

PANEL 01 MAMP 500

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
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
LAF Gas Chromatography, Methamphetamine

GMDN Terms

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

Identifiers

Type ID
Primary 10858904006522
Unit of Use 00858904006525

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius