Identity
- Trade Name
- Echo Pro Table FDA UDI
- Generic Name
- Multi-purpose diagnostic imaging table FDA UDI
- Device Name
- Table, Echocardiography, Echo Pro, 230 VAC FDA UDI
- Model / Reference
- 058-705 FDA UDI
- Description
- Table, Echocardiography, Echo Pro, 230 VAC FDA UDI
Identifiers
- Catalog Number
- 058-705 FDA UDI
- Primary DI / UDI-DI
- 00718175007051 FDA UDI
- FDA Product Code
- FQO FDA UDI
- GMDN Term
- Multi-purpose diagnostic imaging table FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4960 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Echo Pro Table by Biodex Medical Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Biodex Medical Systems
Sources (1)
- FDA UDI 5d794385-f896-436b-8fdb-51c18442330c 35 fields · synced May 30, 2026