FDA UDI In Commercial Distribution 🇺🇸 United States

TrueSpin

DI: 00860001286564 · Model: S001 · MEDTOX DIAGNOSTICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
TrueSpin
Primary DI
00860001286564
Version / Model
S001
Company Name
MEDTOX DIAGNOSTICS, INC.
Labeler DUNS
118569262
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-13
Public Version
1
Public Version Date
2024-12-23
Public Version Status
New
Public Device Record Key
95b88c03-10c7-44f1-991c-00fa66afc687

Device Description

TrueSpin

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use

GMDN Terms

Code Name
36465 General-purpose centrifuge IVD

Identifiers

Type ID
Primary 00860001286564