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.
- Nevro® — Nevro Corporation · Class III
- BIOTRONIK — BIOTRONIK SE & Co. KG · Class III
- Precision Spectra ™ — Boston Scientific Neuromodulation · Class III
- VV-PLUG — Oscor Inc. · Class III
- IS4/DF4 PLUG — Oscor Inc. · Class II
- VV-Plug — Oscor Inc. · Class II
- BS DF-1 — BIOTRONIK SE & Co. KG · Class III
- VV-Plug — Oscor Inc. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- St. Jude Medical, Inc.
Sources (1)
- FDA UDI 99eda95c-6cd7-4393-81cb-1c1066ec0475 37 fields · synced May 30, 2026