FDA UDI In Commercial Distribution 🇺🇸 United States

Consulta® CRT-P

DI: 00613994713667 · Model: C4TR01 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Consulta® CRT-P
Primary DI
00613994713667
Version / Model
C4TR01
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
ee35bcab-7776-4675-94f9-d63ab466f7c2

Device Description

CRT C4TR01 CONSULTA 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
NVZ Pulse generator, permanent, implantable
NKE Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)

GMDN Terms

Code Name
47263 Cardiac resynchronization therapy implantable pacemaker

Identifiers

Type ID
Primary 00613994713667

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P010015 084
P010015 270
P010015 286
P010015 353
P010015 397

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-18 – 55 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
0 – 131 Degrees Fahrenheit