FDA UDI In Commercial Distribution 🇺🇸 United States

eNV®

DI: 00721902321504 · Model: 960-361 · MEDTRONIC NAVIGATION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
eNV®
Primary DI
00721902321504
Version / Model
960-361
Company Name
MEDTRONIC NAVIGATION, INC.
Labeler DUNS
835233107
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-03
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
46d288cf-9d33-4e6d-ba64-6e71cfed64e3

Device Description

FRAME 960-361 FESS

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
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
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
45198 ENT stereotactic surgery system

Identifiers

Type ID
Primary 00721902321504

Customer Contacts