Identity
- Trade Name
- NeuroPace® Patient Data Management System (PDMS) FDA UDI
- Generic Name
- Cannulated surgical drill bit, reusable FDA UDI
- Device Name
- The NeuroPace® Patient Data Management System (PDMS), part of the NeuroPace® RNS® System, is used to store and provide access to historical RNS® Neurostimulator and patient data. The PDMS can also be used to create and simulate detection settings that can be sent to a user identified NeuroPace® Programmer for use at a later date. PDMS is stand-alone software that is accessible via secure internet connection. FDA UDI
- Model / Reference
- Model 4340 FDA UDI
- Description
- The NeuroPace® Patient Data Management System (PDMS), part of the NeuroPace® RNS® System, is used to store and provide access to historical RNS® Neurostimulator and patient data. The PDMS can also be used to create and simulate detection settings that can be sent to a user identified NeuroPace® Programmer for use at a later date. PDMS is stand-alone software that is accessible via secure internet connection. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00855547005007 FDA UDI
- PMA Number
- P100026 FDA UDI
- FDA Product Code
- PFN FDA UDI
- GMDN Term
- Cannulated surgical drill bit, reusable FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cannulated surgical drill bit, reusable
NeuroPace® Patient Data Management System (PDMS) by Neuropace, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
P100026 also covers:
- Connector Cover Kit — Neuropace, Inc.
- Connector Cover Kit — Neuropace, Inc.
- Craniectomy Template Kit — Neuropace, Inc.
- Craniectomy Template Kit — Neuropace, Inc.
- Explant Kit — Neuropace, Inc.
- Ferrule Kit — Neuropace, Inc.
- Ferrule Kit — Neuropace, Inc.
- Magnet — Neuropace, Inc.
- NeuroPace® Cortical Strip Lead Kit — Neuropace, Inc.
- NeuroPace® Cortical Strip Lead Kit — Neuropace, Inc.
- NeuroPace® Cortical Strip Lead Kit — Neuropace, Inc.
- NeuroPace® Cortical Strip Lead Kit — Neuropace, 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
- Neuropace, Inc.
Sources (1)
- FDA UDI e92d4ff7-a081-4bf5-9855-c100ad8b4fff 35 fields · synced Jun 8, 2026