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Attain Performa™ MRI SureScan™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Attain Performa™ MRI SureScan™ FDA UDI
Generic Name
Coronary venous pacing lead FDA UDI
Device Name
LEAD 429888 MRI CANT US FDA UDI
Model / Reference
429888 FDA UDI
Description
LEAD 429888 MRI CANT US FDA UDI

Identifiers

Primary DI / UDI-DI
00643169601833 FDA UDI
PMA Number
P080006 FDA UDI
FDA Product Code
DTB FDA UDI
OJX FDA UDI
GMDN Term
Coronary venous pacing lead FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.3680 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

Yes

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

Dimensions & Sizes

Size
Length — 88.0 Centimeter FDA UDI

Category: Coronary venous pacing lead

Attain Performa™ MRI SureScan™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coronary venous pacing lead.

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 7337cc41-ec7a-41e5-8379-3036338c80e2 37 fields · synced Jun 8, 2026