Identity
- Trade Name
- NMT Monitoring Cable EMG (3.5m) EUDAMEDSTIMPOD FDA UDI
- Generic Name
- Diagnostic peripheral nerve electrical stimulation system FDA UDI
- Device Name
- NMT Monitoring Cable EMG (3.5m) EUDAMEDNMT Monitoring Cable EMG EUDAMEDNeuromuscular blocking agent monitoring cable (3.5m) using electromyography. Accessory to be used with the STIMPOD NMS450 Nerve Stimulator. FDA UDI
- Model / Reference
- XT-45003A EUDAMEDNMT Monitoring Cable EMG (3.5m) FDA UDI
- Description
- Neuromuscular blocking agent monitoring cable (3.5m) using electromyography. Accessory to be used with the STIMPOD NMS450 Nerve Stimulator. FDA UDI
Identifiers
- Catalog Number
- XT45003A FDA UDI
- Primary DI / UDI-DI
- 06009880396696 EUDAMEDFDA UDI
- Basic UDI-DI
- 06009880396XT45003BE EUDAMED
- 510(k) Number
- K213049 FDA UDI
- FDA Product Code
- BXN FDA UDI
- EMDN Code
- Z12062880 NEUROMUSCULAR STIMULATION EQUIPMENT - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Diagnostic peripheral nerve electrical stimulation system FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 868.2775 FDA UDI
- Market of Registration
- Germany EUDAMEDItaly 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
No
FDA UDI
MR Unsafe FDA UDI
NMT Monitoring Cable EMG (3.5m) by Xavant Technology (pty) Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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 | 06009880396XT45003BE | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Xavant Technology (Pty) Ltd
- EUDAMED SRN
- ZA-MF-000011657
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (3)
- EUDAMED 887aa791-f319-4165-a922-66f3c51c22ec 61 fields · synced Jul 16, 2026
- FDA UDI e61a9667-1d20-48db-a01e-cfde4f544fb9 36 fields · synced May 30, 2026
- EUDAMED 84c671ea-88a3-4d25-adf2-53e9a572aa58 61 fields · synced Jul 16, 2026