FDA UDI In Commercial Distribution 🇺🇸 United States

Kitsune

DI: M9702800020080 · Model: 2800-02-008 · Medshape, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kitsune
Primary DI
M9702800020080
Version / Model
2800-02-008
Company Name
Medshape, Inc.
Labeler DUNS
601306413
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-19
Public Version
4
Public Version Date
2020-04-06
Public Version Status
Update
Public Device Record Key
73889a46-5f54-4ee6-9152-4f7f358e40de

Device Description

8mm Staple Drill Guide, reusable, Kitsune

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
LXI Guide, Drill, Ligament

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary M9702800020080