FDA UDI In Commercial Distribution 🇺🇸 United States

Evera™ XT DR

DI: 00763000059569 · Model: DDBB1D1 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Evera™ XT DR
Primary DI
00763000059569
Version / Model
DDBB1D1
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-21
Public Version
7
Public Version Date
2021-06-24
Public Version Status
Update
Public Device Record Key
e073e1bb-f623-40e3-bfe3-1ca05e40f1f6

Device Description

ICD-DR DDBB1D1 EVERA XT US IS1/DF1

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NVZ Pulse generator, permanent, implantable
LWS Implantable cardioverter defibrillator (non-CRT)

GMDN Terms

Code Name
37265 Dual-chamber implantable defibrillator

Identifiers

Type ID
Primary 00763000059569

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 131 Degrees Fahrenheit