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Sjm™

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
SJM™ FDA UDI
Generic Name
Neural-tissue electrical stimulation lead adaptor FDA UDI
Device Name
Multilead Trial Cable FDA UDI
Model / Reference
3014 FDA UDI
Description
Multilead Trial Cable FDA UDI

Identifiers

Catalog Number
3014 FDA UDI
Primary DI / UDI-DI
05415067024015 FDA UDI
PMA Number
P140009 FDA UDI
FDA Product Code
MHY FDA UDI
GMDN Term
Neural-tissue electrical stimulation lead adaptor 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Neural-tissue electrical stimulation lead adaptor

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

Similar devices

Also classified as Neural-tissue electrical stimulation lead adaptor.

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 aab5ab26-2fb0-44e2-9c66-fc18a5f34d0c 37 fields · synced Jun 8, 2026