Identity
- Trade Name
- sEEG DEPTHALON® FDA UDI
- Generic Name
- Depth electrode FDA UDI
- Device Name
- SEEG DEPTH ELECTRODE, 16 CONTACT, 17.8mm RECORDING LENGTH, 2mm BULLET TIP, 0.5 PLATINUM CONTACTS, NO CONN, REMOVABLE STYL FDA UDI
- Model / Reference
- 2102-16-188 FDA UDI
- Description
- SEEG DEPTH ELECTRODE, 16 CONTACT, 17.8mm RECORDING LENGTH, 2mm BULLET TIP, 0.5 PLATINUM CONTACTS, NO CONN, REMOVABLE STYL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00650551004899 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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Depth electrode
sEEG DEPTHALON® by Pmt Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Pmt Corp.
Sources (1)
- FDA UDI 018c600f-9a20-4ad5-bb69-62c75cefac42 33 fields · synced Jun 8, 2026