FDA UDI In Commercial Distribution 🇺🇸 United States

Medtronic Reusable Instruments

DI: 00613994245120 · Model: X1103512 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medtronic Reusable Instruments
Primary DI
00613994245120
Version / Model
X1103512
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
b1e07240-acfb-4f5c-a07f-b6f311586459

Device Description

INSTRUMENT X1103512 BAYONETD HK SHRP 3MM

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
HXB PROBE
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
47779 Orthopaedic instrument surgical connector

Identifiers

Type ID
Primary 00613994245120

Customer Contacts