Identity
- Trade Name
- SlimTip™ FDA UDI
- Generic Name
- Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection FDA UDI
- Device Name
- DRG Trial Lead Kit FDA UDI
- Model / Reference
- MN10350-90A FDA UDI
- Description
- DRG Trial Lead Kit FDA UDI
Identifiers
- Catalog Number
- MN10350-90A FDA UDI
- Primary DI / UDI-DI
- 05415067027146 FDA UDI
- PMA Number
- P150004 FDA UDI
- FDA Product Code
- PMP FDA UDI
- GMDN Term
- Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Length — 90.0000 Centimeter FDA UDI
SlimTip™ by Advanced Neuromodulation Systems — 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 lead, wired connection.
- PISCES-QUAD PLUS ™ — MEDTRONIC, INC. · Class III
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- Nevro® — Nevro Corporation · Class III
- Artisan™ — Boston Scientific Neuromodulation · Class III
- Altius Cuff Large — Neuros Medical, Inc. · Class III
- Lamitrode Tripole™ — ST. JUDE MEDICAL, INC. · Class III
- Nalu Medical, Inc. — NALU MEDICAL · Class II
- Nalu Medical, Inc. — NALU MEDICAL · Class II
Cleared under the same submission
P150004 also covers:
- NeuroSphere™ — Advanced Neuromodulation Systems
- Proclaim™ — Advanced Neuromodulation Systems
- SlimTip™ — Advanced Neuromodulation Systems
- SlimTip™ — Advanced Neuromodulation Systems
- SlimTip™ — Advanced Neuromodulation Systems
- Axium™ — SPINAL MODULATION, INC.
- Axium™ — SPINAL MODULATION, INC.
- Axium™ — SPINAL MODULATION, INC.
- Axium™ — SPINAL MODULATION, INC.
- Axium™ — SPINAL MODULATION, INC.
- Axium™ — SPINAL MODULATION, INC.
- Axium™ — SPINAL MODULATION, 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
- Advanced Neuromodulation Systems
Sources (1)
- FDA UDI 099d0ecc-c0ee-44ca-bea7-dde690b24ba1 38 fields · synced May 30, 2026