FDA UDI In Commercial Distribution 🇺🇸 United States

Medtronic

DI: 00763000401184 · Model: 9735669R · MEDTRONIC NAVIGATION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medtronic
Primary DI
00763000401184
Version / Model
9735669R
Company Name
MEDTRONIC NAVIGATION, INC.
Labeler DUNS
835233107
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-16
Public Version
1
Public Version Date
2024-12-24
Public Version Status
New
Public Device Record Key
59725d9b-8a0f-4959-a722-f43e0664fac7

Device Description

S8 MAIN ENT SYSTEM REFURB 9735669R

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
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
No

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
45199 Multi-purpose stereotactic surgery system

Identifiers

Type ID
Primary 00763000401184

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162309 000