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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
Implantable pulse generator port plug FDA UDI
Device Name
DF-1 (3.2 mm) RECEPTACLE PLUG FDA UDI
Model / Reference
AC-DP-3 FDA UDI
Description
DF-1 (3.2 mm) RECEPTACLE PLUG FDA UDI

Identifiers

Catalog Number
AC-DP-3 FDA UDI
Primary DI / UDI-DI
05414734500258 FDA UDI
FDA Product Code
LWS FDA UDI
GMDN Term
Implantable pulse generator port plug 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

Dimensions & Sizes

Size
Outer Diameter — 3.2 Millimeter FDA UDI

Category: Implantable pulse generator port plug

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

Similar devices

Also classified as Implantable pulse generator port plug.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 99eda95c-6cd7-4393-81cb-1c1066ec0475 37 fields · synced May 30, 2026