FDA UDI In Commercial Distribution 🇺🇸 United States

ClearView Uterine Manipulator

DI: 00814247020604 · Model: UM900 · CLINICAL INNOVATIONS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ClearView Uterine Manipulator
Primary DI
00814247020604
Version / Model
UM900
Company Name
CLINICAL INNOVATIONS, LLC
Labeler DUNS
809524291
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-01
Public Version
4
Public Version Date
2018-12-07
Public Version Status
Update
Public Device Record Key
ed1a94a4-85ea-4387-96a5-8e42d825c176

Device Description

ClearView Uterine Manipulator, 9cm

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
Yes
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 20814247020608
Package 10814247020601
Primary 00814247020604

Premarket Submissions

Submission Number Supplement Number
K940681 000