FDA UDI In Commercial Distribution 🇺🇸 United States

VERTEX MAX™

DI: 00613994372017 · Model: 9733519 · MEDTRONIC NAVIGATION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
VERTEX MAX™
Primary DI
00613994372017
Version / Model
9733519
Company Name
MEDTRONIC NAVIGATION, INC.
Labeler DUNS
835233107
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-27
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
477a3287-dbce-481c-9478-07cdc2b1930e

Device Description

BIT 9733519 3.0mm CANNULATED STERILE

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
43962 Drilling power tool attachment, basic

Identifiers

Type ID
Primary 00613994372017

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 3.0 Millimeter