FDA UDI In Commercial Distribution 🇺🇸 United States

EnVeo™ PRO

DI: 00643169987180 · Model: L-ENVPRO-16-US · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EnVeo™ PRO
Primary DI
00643169987180
Version / Model
L-ENVPRO-16-US
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-28
Public Version
6
Public Version Date
2022-07-04
Public Version Status
Update
Public Device Record Key
289cf743-a31b-44a8-b687-7ed591413327

Device Description

LOAD SYS L-ENVPRO-16-US

Device Characteristics

Single Use
Yes
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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NPT Aortic valve, prosthesis, percutaneously delivered

GMDN Terms

Code Name
60245 Aortic transcatheter heart valve bioprosthesis, stent-like framework

Identifiers

Type ID
Primary 00643169987180

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P130021 043
P130021 072
P130021 083

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store the catheter and LS in a cool, dry environment.