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Assurity MRI™

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
Assurity MRI™ FDA UDI
Generic Name
Single-chamber implantable pacemaker, rate-responsive FDA UDI
Device Name
SR Pacemaker SSIR FDA UDI
Model / Reference
PM1272 FDA UDI
Description
SR Pacemaker SSIR FDA UDI

Identifiers

Catalog Number
PM1272 FDA UDI
Primary DI / UDI-DI
05414734509572 FDA UDI
PMA Number
P140033 FDA UDI
FDA Product Code
LWP FDA UDI
GMDN Term
Single-chamber implantable pacemaker, rate-responsive 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Single-chamber implantable pacemaker, rate-responsive

Assurity MRI™ by St. Jude Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Single-chamber implantable pacemaker, rate-responsive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fc17081f-888b-4cf6-bf95-641cac23d721 37 fields · synced Jun 8, 2026