FDA UDI In Commercial Distribution 🇺🇸 United States

TOX II_09 24

DI: B800TOXII09240 · Model: TOX II_09 24 · UTAK LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TOX II_09 24
Primary DI
B800TOXII09240
Version / Model
TOX II_09 24
Catalog Number
TOX II_09 24
Company Name
UTAK LABORATORIES, INC.
Labeler DUNS
092519016
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-20
Public Version
1
Public Version Date
2024-06-28
Public Version Status
New
Public Device Record Key
ffa2ee1b-47b6-4054-a722-75184edaf371

Device Description

TOX II_09 24

Device Characteristics

Single Use
No
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
Yes
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
LAS Drug Specific Control Materials

GMDN Terms

Code Name
55461 Multiple drugs of abuse IVD, control

Identifiers

Type ID
Package B800TOXII09245
Primary B800TOXII09240

Customer Contacts

Phone
8888825522

Device Sizes

Type Value Unit Text
Total Volume 1 Milliliter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– -10 Degrees Celsius