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Protektor32 Pods and Pod Kit
EUDAMEDFDA UDIClass I (EU MDR)
Ref 017885Ref 002934Ref 021057Ref 017900
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 POD 2 (E-H) - 1' FDA UDI
- Model / Reference
- 017885 EUDAMEDFDA UDI002934 EUDAMED021057 EUDAMED017900 EUDAMED
- Description
- P32-STIM POD 2 (E-H) - 1' FDA UDI
Identifiers
- Catalog Number
- 017885 FDA UDI
- Primary DI / UDI-DI
- 00382830046312 EUDAMEDFDA UDI00382830060141 EUDAMED00382830047302 EUDAMED00382830047296 EUDAMED
- Basic UDI-DI
- 038283NA00095EQ EUDAMED
- Direct Marketing DI
- 00382830046312 EUDAMED00382830060141 EUDAMED00382830047302 EUDAMED00382830047296 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
Category: Auditory stimulator
Protektor32 Pods and Pod Kit by Natus Medical Incorporated Dba Excel-Tech Ltd (xltek) — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
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Also classified as Auditory stimulator.
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- GN Otometrics A/S — Natus Medical Denmark ApS · Class II
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 (5)
- EUDAMED e4c40701-b65b-49f0-b8af-7fb9e53be5ca 61 fields · synced Jul 10, 2026
- EUDAMED f61a650e-1de0-4959-9cb9-8410e4176f66 61 fields · synced May 17, 2026
- EUDAMED ea09ec31-fed6-4ca4-928f-4dab389e5301 61 fields · synced May 17, 2026
- EUDAMED 95648731-bdc0-4d70-a85b-1fa2545a40dd 61 fields · synced May 18, 2026
- FDA UDI f4b2e9b3-70d2-4e66-8a1b-279f825ebbed 36 fields · synced May 30, 2026