FDA UDI In Commercial Distribution 🇺🇸 United States

BENZODIAZEPINES +25%

DI: B80003716500090 · Model: BENZO +25 PM · UTAK LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
7
Pkg Device Count
1

Basic Information

Brand Name
BENZODIAZEPINES +25%
Primary DI
B80003716500090
Version / Model
BENZO +25 PM
Company Name
UTAK LABORATORIES, INC.
Labeler DUNS
092519016
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-15
Public Version
1
Public Version Date
2022-08-23
Public Version Status
New
Public Device Record Key
686b6fdb-c633-45a7-a6b6-3751e47c4ed7

Device Description

BENZODIAZEPINES +25%

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
55527 Benzodiazepine group IVD, control

Identifiers

Type ID
Package B80003716500091
Primary B80003716500090
Package B80003716500092
Package B80003716500093
Package B80003716500096
Package B80003716500097
Package B80003716500098

Customer Contacts