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Sound Pro Table

FDA UDI

Class I (US FDA UDI)

by Biodex Medical Systems

Identity

Trade Name
Sound Pro Table FDA UDI
Generic Name
Multi-purpose diagnostic imaging table FDA UDI
Device Name
Table, Combination, Sound Pro, 230 VAC FDA UDI
Model / Reference
058-715 FDA UDI
Description
Table, Combination, Sound Pro, 230 VAC FDA UDI

Identifiers

Catalog Number
058-715 FDA UDI
Primary DI / UDI-DI
00718175007150 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

Sound 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

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Manufacturer

Sources (1)

  • FDA UDI 93dd7bc2-b9d3-4794-8d5e-ce3f7a5d8040 35 fields · synced Jun 8, 2026