FDA UDI In Commercial Distribution 🇺🇸 United States

Medtronic Reusable Instruments

DI: 00643169371675 · Model: X1011072 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medtronic Reusable Instruments
Primary DI
00643169371675
Version / Model
X1011072
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-07
Public Version
1
Public Version Date
2022-10-17
Public Version Status
New
Public Device Record Key
07999d71-62c9-4345-82c7-3f5463262b6b

Device Description

KERRISON X1011072 2MM BAYONETED CURVED

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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00643169371675

Customer Contacts