Spiderview / Spiderflash
FDA UDIEUDAMEDClass II (US FDA UDI)
Identity
- Trade Name
- RC013 EUDAMEDSPIDERVIEW / SPIDERFLASH FDA UDI
- Generic Name
- Electrocardiographic lead set, reusable FDA UDI
- Model / Reference
- ECG cables EUDAMEDRC013 EUDAMED2 Leads / 3E FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08031527015057 EUDAMEDFDA UDI
- Basic UDI-DI
- 8031527ECGCABLES0000001E5 EUDAMED
- FDA Product Code
- MWJ FDA UDI
- EMDN Code
- Z12050403 ECG HOLTER RECORDERS EUDAMED
- GMDN Term
- Electrocardiographic lead set, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 870.2800 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Category: Electrocardiographic lead set, reusable
Spiderview / Spiderflash by Microport Crm Srl — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Electrocardiographic lead set, reusable.
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Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Microport Crm Srl
Sources (2)
- FDA UDI 85a5c7cf-beb1-4c5d-a946-e74d386c46ee 32 fields · synced Aug 1, 2026
- EUDAMED 24054d11-8df8-4cf1-95da-56e8cafd97a5 61 fields · synced Jun 18, 2026