← Back to catalogue
Eclipse Pro, Cable, Px, 3 Snap, Long
EUDAMEDFDA UDIClass I (EU MDR)
Ref 700-0372-00Model Eclipse Pro cables and patches
Identity
- Trade Name
- ECLIPSE PRO,CABLE,PX,3 SNAP,LONG EUDAMEDEclipse Pro FDA UDI
- Generic Name
- Electrical-only medical device connection cable, reusable FDA UDI
- Device Name
- Eclipse Pro cables and patches EUDAMEDECLIPSE PRO,CABLE,PX,3 SNAP,LONG FDA UDI
- Model / Reference
- Eclipse Pro cables and patches EUDAMED700-0372-00 EUDAMEDEclipse Pro FDA UDI
- Description
- ECLIPSE PRO,CABLE,PX,3 SNAP,LONG FDA UDI
Identifiers
- Catalog Number
- 700-0372-00 FDA UDI
- Primary DI / UDI-DI
- 10841522127236 EUDAMEDFDA UDI
- Basic UDI-DI
- 08415221IEPROC&POWN7U EUDAMED
- FDA Product Code
- MWJ FDA UDI
- EMDN Code
- Z12050485 HOLTER SYSTEM INSTRUMENTS FOR CARDIOVASCULAR PARAMETERS - CONSUMABLES EUDAMED
- GMDN Term
- Electrical-only medical device connection cable, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 870.2800 FDA UDI
- Market of Registration
- France 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
Eclipse Pro, Cable, Px, 3 Snap, Long by Spacelabs Healthcare 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 | 08415221IEPROC&POWN7U | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Spacelabs Healthcare Ltd
- EUDAMED SRN
- GB-MF-000001196
- Authorised Representative
- MediMark Europe Sarl. FR-AR-000000182
Sources (2)
- EUDAMED cc026b40-2e1f-4c36-8d8d-d0215c737be6 61 fields · synced Jul 29, 2026
- FDA UDI fa31c415-73ae-402c-a258-fd1e99169031 34 fields · synced May 27, 2026