FDA UDI In Commercial Distribution 🇺🇸 United States

OPIATES 500 NG/ML

DI: B80004830000010 · Model: OPIA 500 U · UTAK LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
7
Pkg Device Count
1

Basic Information

Brand Name
OPIATES 500 NG/ML
Primary DI
B80004830000010
Version / Model
OPIA 500 U
Company Name
UTAK LABORATORIES, INC.
Labeler DUNS
092519016
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-25
Public Version
1
Public Version Date
2022-05-03
Public Version Status
New
Public Device Record Key
f90a4c2c-cade-477d-b3d6-90d720f3b865

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
Primary B80004830000010
Package B80004830000011
Package B80004830000012
Package B80004830000013
Package B80004830000016
Package B80004830000017
Package B80004830000018

Customer Contacts