FDA UDI In Commercial Distribution 🇺🇸 United States

FENTANYL PLUS LEVEL 2

DI: B80003716500040 · Model: FENT+ 2 U PM · UTAK LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
7
Pkg Device Count
1

Basic Information

Brand Name
FENTANYL PLUS LEVEL 2
Primary DI
B80003716500040
Version / Model
FENT+ 2 U PM
Company Name
UTAK LABORATORIES, INC.
Labeler DUNS
092519016
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-16
Public Version
1
Public Version Date
2022-06-24
Public Version Status
New
Public Device Record Key
7b024c65-ddb4-4747-b404-e98e9dd027ff

Device Description

FENTANYL PLUS LEVEL 2

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
55723 Opiate/opiate metabolite IVD, control

Identifiers

Type ID
Package B80003716500041
Primary B80003716500040
Package B80003716500042
Package B80003716500043
Package B80003716500046
Package B80003716500047
Package B80003716500048

Customer Contacts