Identity
- Trade Name
- Tennafix™ FDA UDI
- Generic Name
- Cable/lead/sensor non-conductive skin-adherent patch, single-use FDA UDI
- Device Name
- Adhesive Pads FDA UDI
- Model / Reference
- 1205 FDA UDI
- Description
- Adhesive Pads FDA UDI
Identifiers
- Catalog Number
- 1205 FDA UDI
- Primary DI / UDI-DI
- 05414734400749 FDA UDI
- PMA Number
- P010032 FDA UDI
- FDA Product Code
- LGW FDA UDI
- GMDN Term
- Cable/lead/sensor non-conductive skin-adherent patch, single-use FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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: Cable/lead/sensor non-conductive skin-adherent patch, single-use
Tennafix™ by St. Jude Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
P010032 also covers:
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- Lamitrode® — Advanced Neuromodulation Systems
- Lamitrode® — Advanced Neuromodulation Systems
- Quattrode® — Advanced Neuromodulation Systems
- Quattrode® — Advanced Neuromodulation Systems
- Eon C™ — ST. JUDE MEDICAL, INC.
- Eon Mini™ — ST. JUDE MEDICAL, INC.
- Eon Mini™ — ST. JUDE MEDICAL, INC.
- Eon™ — ST. JUDE MEDICAL, INC.
- Exclaim™ — ST. JUDE MEDICAL, INC.
- Exclaim™ — ST. JUDE MEDICAL, INC.
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 4e7021e3-4bc2-4127-adb1-f039a0170af7 37 fields · synced May 30, 2026