FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00763000578497 · Model: 9736082 · MEDTRONIC NAVIGATION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00763000578497
Version / Model
9736082
Company Name
MEDTRONIC NAVIGATION, INC.
Labeler DUNS
835233107
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-04
Public Version
1
Public Version Date
2021-12-13
Public Version Status
New
Public Device Record Key
7a343914-0059-4df5-acbd-c7a44b43175d

Device Description

KIT 9736082 S8 FPU SPINAL FUSION W O-ARM

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
PM Exempt
No
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
No

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
45200 Orthopaedic stereotactic surgery system

Identifiers

Type ID
Primary 00763000578497

Customer Contacts