Identity
- Trade Name
- microTargeting™ Electrode Lead Cable FDA UDI
- Generic Name
- Depth electrode FDA UDI
- Device Name
- Guidline 4000 ™ 5.0 1.5m Special-use Lead, 1x For use with microTargeting ™ Electrodes FDA UDI
- Model / Reference
- C0232-00781 FDA UDI
- Description
- Guidline 4000 ™ 5.0 1.5m Special-use Lead, 1x For use with microTargeting ™ Electrodes FDA UDI
Identifiers
- Catalog Number
- C0232 FDA UDI
- Primary DI / UDI-DI
- 00873263007815 FDA UDI
- 510(k) Number
- K183123 FDA UDI
- FDA Product Code
- GZL FDA UDI
- GMDN Term
- Depth electrode FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1330 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Length — 1.5 Meter FDA UDI
Category: Depth electrode
microTargeting™ Electrode Lead Cable by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K183123 also covers:
- Guideline 4000 5.0™ 3m Interface Cable — FHC, INC.
- Guideline 4000 5.0™ Interface — FHC, INC.
- Guideline 4000 5.0™ LF Interface — FHC, INC.
- Guideline 4000 5.0™ Motor & Encoder — FHC, INC.
- Guideline 4000 5.0™ microTargeting™ Controller Card — FHC, INC.
- Guideline 4000 5.0™ microTargeting™ Interface Card — FHC, INC.
- Guideline 4000™ 5.0 — FHC, INC.
- Guideline 4000™ 5.0 — FHC, INC.
- Guideline 4000™ 5.0 — FHC, INC.
- Guideline 4000™ 5.0 — FHC, INC.
- Guideline 4000™ 5.0 Accessory — FHC, INC.
- Lead Adapter Cable — FHC, 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Fhc, Inc.
Sources (1)
- FDA UDI fddbb809-7da0-4920-9818-77a8a0e070dd 38 fields · synced May 30, 2026