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Natus Quantum REF Jumper Cable, 3ft
EUDAMEDFDA UDIFDA 510(k)Class I (EU MDR)
Ref 014883
Identity
- Trade Name
- Natus Quantum REF Jumper Cable, 3ft EUDAMEDNatus FDA UDI
- Generic Name
- Electrical-only medical device connection cable, reusable FDA UDI
- Device Name
- Quantum II Class I Accessories EUDAMEDNatus Quantum REF Jumper Cable, 3ft FDA UDI
- Model / Reference
- 014883 EUDAMEDFDA UDI
- Description
- Natus Quantum REF Jumper Cable, 3ft FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00382830016469 EUDAMEDFDA UDI
- Basic UDI-DI
- 038283NA00056EE EUDAMED
- Direct Marketing DI
- 00382830016469 EUDAMED
- FDA Product Code
- GXY FDA UDI
- EMDN Code
- V0880 MEDICAL SUPPORT EQUIPMENT - ACCESSORIES EUDAMED
- GMDN Term
- Electrical-only medical device connection cable, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 882.1320 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Natus Quantum REF Jumper Cable, 3ft by Natus Medical Incorporated Dba Excel-Tech Ltd (xltek) — Class I — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA…
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K180181 | Class I | Active |
| FDA 510(k) | United States | FDA_510K | K143440 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 038283NA00056EE | Class I | Active |
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Manufacturer
- EUDAMED SRN
- CA-MF-000004001
- Authorised Representative
- Natus Manufacturing Ltd IE-AR-000000884
Sources (3)
- EUDAMED 40d55164-23bf-4aca-a66e-2866d0893210 61 fields · synced Oct 6, 2026
- FDA UDI d1ca45c6-bf55-42d8-b46b-bb4126f8a6d7 33 fields · synced May 29, 2026
- FDA 510(k) K180181 1 fields · synced May 18, 2026