Identity
- Trade Name
- Protektor32 Pods and Pod Kit EUDAMEDXltek FDA UDI
- Generic Name
- Electromyograph FDA UDI
- Device Name
- P32 ACQ Pod combine kit EUDAMEDP32 - STIM Extension cable 2 (E-H) - 9' FDA UDI
- Model / Reference
- 017869 EUDAMEDFDA UDI
- Description
- P32 - STIM Extension cable 2 (E-H) - 9' FDA UDI
Identifiers
- Catalog Number
- 017869 FDA UDI
- Primary DI / UDI-DI
- 00382830046190 EUDAMEDFDA UDI
- Basic UDI-DI
- 038283NA00095EQ EUDAMED
- Direct Marketing DI
- 00382830046190 EUDAMED
- 510(k) Number
- K093304 FDA UDI
- FDA Product Code
- GWF FDA UDI
- EMDN Code
- Z129013 GENERAL AUDITORY AND/OR VISUAL STIMULATORS EUDAMED
- GMDN Term
- Electromyograph FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 882.1870 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Protektor32 Pods and Pod Kit by Natus Medical Incorporated Dba Excel-Tech Ltd (xltek) — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 038283NA00095EQ | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- EUDAMED SRN
- CA-MF-000004001
- Authorised Representative
- Natus Manufacturing Ltd IE-AR-000000884
Sources (2)
- EUDAMED a38e57ee-c623-4728-a227-8e4899108f8e 61 fields · synced Jun 17, 2026
- FDA UDI 16327f0f-9017-4c31-8511-31609f3b60f8 36 fields · synced May 30, 2026