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EchoBed X

FDA UDI

Class I (US FDA UDI)

by Medical Positioning, Inc.

Identity

Trade Name
EchoBed X FDA UDI
Generic Name
Multi-purpose diagnostic imaging table FDA UDI
Device Name
EchoBed X, H-F, 2D FDA UDI
Model / Reference
222 FDA UDI
Description
EchoBed X, H-F, 2D FDA UDI

Identifiers

Primary DI / UDI-DI
00848871000954 FDA UDI
FDA Product Code
LGX 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
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

No

FDA UDI

Category: Multi-purpose diagnostic imaging table

EchoBed X by Medical Positioning, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose diagnostic imaging table.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 00c33c41-4bfc-4a8c-8940-27ee0bb699f3 34 fields · synced Jun 9, 2026