FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00885074056487 · Model: 9450058 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00885074056487
Version / Model
9450058
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-17
Public Version
4
Public Version Date
2023-11-02
Public Version Status
Update
Public Device Record Key
e19624f8-2217-473b-95de-2c841f2f7842

Device Description

CAPITAL 9450058 NIM CNTRL PATIENT INT BX

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
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
IKN Electromyograph, diagnostic
ETN STIMULATOR, NERVE
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE

GMDN Terms

Code Name
35723 Nerve-locating system

Identifiers

Type ID
Primary 00885074056487

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K031510 000