FDA UDI In Commercial Distribution 🇺🇸 United States

Viva™ CRT-P

DI: 00643169351905 · Model: C6TR01 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Viva™ CRT-P
Primary DI
00643169351905
Version / Model
C6TR01
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
5
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
3a55a46d-29b7-470e-a1ef-7fee9c8060e3

Device Description

CRT C6TR01 VIVA CRT-P US MR

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
NKE Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)

GMDN Terms

Code Name
47263 Cardiac resynchronization therapy implantable pacemaker

Identifiers

Type ID
Primary 00643169351905

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P010015 227
P010015 270
P010015 286
P010015 353
P010015 397

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 131 Degrees Fahrenheit