FDA UDI In Commercial Distribution 🇺🇸 United States

Kronner Manipujector

DI: 00888937015805 · Model: 6003 · Coopersurgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kronner Manipujector
Primary DI
00888937015805
Version / Model
6003
Company Name
Coopersurgical, Inc.
Labeler DUNS
801895244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-31
Public Version
6
Public Version Date
2024-02-28
Public Version Status
Update
Public Device Record Key
894bd4ac-5171-4b7c-9813-bab6e4504e6b

Device Description

Uterine manipulator

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
HES Insufflator, Carbon-Dioxide, Uterotubal (And Accessories)

GMDN Terms

Code Name
58051 Uterine manipulator, single-use

Identifiers

Type ID
Primary 00888937015805
Package 20888937015809

Premarket Submissions

Submission Number Supplement Number
K904473 000

Device Sizes

Type Value Unit Text
Outer Diameter 5 Millimeter
Length 33 Centimeter