← Back to catalogue
Natus Elite v2 Software Upgrade with New System Order
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref 688-630200
Identity
- Trade Name
- Natus Elite v2 Software Upgrade with New System Order EUDAMEDNatus FDA UDI
- Generic Name
- Electromyograph FDA UDI
- Device Name
- Nicolet EDX EUDAMEDNatus Elite v2 Software Upgrade with New System Order FDA UDI
- Model / Reference
- 688-630200 EUDAMEDFDA UDI
- Description
- Natus Elite v2 Software Upgrade with New System Order FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00382830062251 EUDAMEDFDA UDI
- Basic UDI-DI
- 038283NA00151E9 EUDAMED
- FDA Product Code
- GWF FDA UDI
- EMDN Code
- Z12100482 ELECTROMYOGRAPHY INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED
- GMDN Term
- Electromyograph FDA UDI
Classification
- Device Class
- Class IIb 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
Natus Elite v2 Software Upgrade with New System Order by Natus Neurology Incorporated — Class IIb — 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 | 038283NA00151E9 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Natus Neurology Incorporated
- EUDAMED SRN
- US-MF-000004246
- Authorised Representative
- Natus Manufacturing Ltd IE-AR-000000884
Sources (2)
- EUDAMED bae61502-31a3-4e2c-acca-38680aad2613 61 fields · synced Oct 6, 2026
- FDA UDI a165ac22-3350-43ed-b576-48bd10d2690a 33 fields · synced May 29, 2026