FDA UDI In Commercial Distribution 🇺🇸 United States

Percepta™ CRT-P MRI SureScan™

DI: 00643169735637 · Model: W1TR01 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Percepta™ CRT-P MRI SureScan™
Primary DI
00643169735637
Version / Model
W1TR01
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-18
Public Version
9
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
b19ab068-f00c-42e0-a99b-9af0e5605dbe

Device Description

CRTP W1TR01 PERCEPTA CRTP MRI US

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
MR Conditional
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 00643169735637

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P010015 317
P010015 338
P010015 340
P010015 357
P010015 391
P010015 399
P010015 411
P010015 439

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 131 Degrees Fahrenheit