FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00852073002630 · Model: K-UMI · C R I
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00852073002630
Version / Model
K-UMI
Catalog Number
TMI6003
Company Name
C R I
Labeler DUNS
130814890
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-10
Public Version
4
Public Version Date
2018-12-07
Public Version Status
Update
Public Device Record Key
7a87beab-8428-4e86-8d44-8419dc13c3f7

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 10852073002637
Primary 00852073002630

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K974357 000

Device Sizes

Type Value Unit Text
Length 33 Centimeter
Outer Diameter 5 Millimeter