FDA UDI In Commercial Distribution 🇺🇸 United States

KMI IMI GROUP

DI: 00851314007120 · Model: 19-0093 · Innovative Med
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KMI IMI GROUP
Primary DI
00851314007120
Version / Model
19-0093
Company Name
Innovative Med
Labeler DUNS
928308407
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-30
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
70c0c05a-5b62-444c-9b65-aec944ddf2c3

Device Description

Dissectors & Disruptors

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GDI Dissector, Surgical, General & Plastic Surgery

GMDN Terms

Code Name
11290 Open-surgery dissector

Identifiers

Type ID
Primary 00851314007120

Customer Contacts

Phone
949-458-1897