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Percepta™ CRT-P MRI SureScan™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Percepta™ CRT-P MRI SureScan™ FDA UDI
Generic Name
Cardiac resynchronization therapy implantable pacemaker FDA UDI
Device Name
CRTP W1TR01 PERCEPTA CRTP MRI US FDA UDI
Model / Reference
W1TR01 FDA UDI
Description
CRTP W1TR01 PERCEPTA CRTP MRI US FDA UDI

Identifiers

Primary DI / UDI-DI
00643169891401 FDA UDI
PMA Number
P010015 FDA UDI
FDA Product Code
NKE FDA UDI
GMDN Term
Cardiac resynchronization therapy implantable pacemaker FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Cardiac resynchronization therapy implantable pacemaker

Percepta™ CRT-P MRI SureScan™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac resynchronization therapy implantable pacemaker.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 91e39384-46e0-40a5-bd7e-84085b8f1659 36 fields · synced May 30, 2026