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Infinity™

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
Infinity™ FDA UDI
Generic Name
Deep brain electrical stimulation system FDA UDI
Device Name
Implantable Pulse Generator FDA UDI
Model / Reference
6662 FDA UDI
Description
Implantable Pulse Generator FDA UDI

Identifiers

Catalog Number
6662 FDA UDI
Primary DI / UDI-DI
05415067020260 FDA UDI
PMA Number
P140009 FDA UDI
FDA Product Code
MHY FDA UDI
GMDN Term
Deep brain electrical stimulation system 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Deep brain electrical stimulation system

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

Similar devices

Also classified as Deep brain electrical stimulation system.

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 65ab81d0-61a1-4c58-9222-8fc04936b514 37 fields · synced May 30, 2026