FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00613994403896 · Model: 9297009 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00613994403896
Version / Model
9297009
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-17
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
cd4639f5-714e-47a9-9dac-fb549331012f

Device Description

HANDLE 9297009 MICRO TRIAL

Device Characteristics

Single Use
No
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
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
44869 Orthopaedic graft inserter

Identifiers

Type ID
Primary 00613994403896

Customer Contacts