FDA UDI In Commercial Distribution 🇺🇸 United States

Uterine ElevatOR Pro

DI: 09349967002780 · Model: UE-TVPRO-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
Primary DI
09349967002780
Version / Model
UE-TVPRO-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
2018-01-31
Public Version
4
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
71a7ee8c-fd1e-4e8f-b8c1-c1e69803566c

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 09349967002803
Package 09349967002797
Primary 09349967002780

Device Sizes

Type Value Unit Text
Outer Diameter 35 Millimeter