FDA UDI In Commercial Distribution 🇺🇸 United States

STOCK 2

DI: B80010095200030 · Model: STK 2 WB V2 BD 22 · UTAK LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
7
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
STOCK 2
Primary DI
B80010095200030
Version / Model
STK 2 WB V2 BD 22
Company Name
UTAK LABORATORIES, INC.
Labeler DUNS
092519016
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-09
Public Version
2
Public Version Date
2022-08-19
Public Version Status
Update
Public Device Record Key
013c4403-70ff-46f5-b20c-47d6f83bf5ae

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
54714 Multiple heavy metal IVD, control

Identifiers

Type ID
Primary B80010095200030
Package B80010095200031
Package B80010095200032
Package B80010095200033
Package B80010095200036
Package B80010095200037
Package B80010095200038

Customer Contacts