FDA UDI In Commercial Distribution 🇺🇸 United States

Uterine ElevatOR Pro with OccludOR Balloon

DI: 09349967003329 · Model: UE-OBPRO-35 · 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
09349967003329
Version / Model
UE-OBPRO-35
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
2019-03-07
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
c4fd04fd-26c7-44df-975a-9b3e79255102

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 09349967003343
Package 09349967003336
Primary 09349967003329

Device Sizes

Type Value Unit Text
Outer Diameter 32 Millimeter