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Protégé™

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
Protégé™ FDA UDI
Generic Name
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable FDA UDI
Device Name
IPG, 16-Channel Rechargeable FDA UDI
Model / Reference
3789 FDA UDI
Description
IPG, 16-Channel Rechargeable FDA UDI

Identifiers

Catalog Number
3789 FDA UDI
Primary DI / UDI-DI
05415067020833 FDA UDI
PMA Number
P010032 FDA UDI
FDA Product Code
LGW FDA UDI
GMDN Term
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable 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: Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable

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

Similar devices

Also classified as Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable.

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 6248cc5c-c32d-41b5-800c-f1334de02a83 37 fields · synced May 30, 2026