FDA UDI In Commercial Distribution 🇺🇸 United States

Uterine ElevatOR PRO with OccludOR Balloon™

DI: 09349967004982 · Model: UE-OBPRO-40NT · THE O R COMPANY PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Uterine ElevatOR PRO with OccludOR Balloon™
Primary DI
09349967004982
Version / Model
UE-OBPRO-40NT
Catalog Number
UE-OBPRO-40NT
Company Name
THE O R COMPANY PTY LTD
Labeler DUNS
744346235
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-26
Public Version
1
Public Version Date
2023-06-05
Public Version Status
New
Public Device Record Key
cb487057-a203-417a-aac2-7bbf43a53eb0

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LKF Cannula, Manipulator/Injector, Uterine

GMDN Terms

Code Name
58051 Uterine manipulator, single-use

Identifiers

Type ID
Package 19349967004989
Primary 09349967004982
Package 29349967004986

Device Sizes

Type Value Unit Text
Outer Diameter 40 Millimeter