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Allegro Imaging Table 120V, 60HZ

FDA UDI

Class II (US FDA UDI)

by Mizuho Orthopedic Systems, Inc.

Identity

Trade Name
Allegro Imaging Table 120V, 60HZ FDA UDI
Generic Name
Multi-purpose diagnostic imaging table FDA UDI
Device Name
Allegro® Mobile Imaging Table FDA UDI
Model / Reference
6800 FDA UDI
Description
Allegro® Mobile Imaging Table FDA UDI

Identifiers

Catalog Number
6800 FDA UDI
Primary DI / UDI-DI
00842430100017 FDA UDI
FDA Product Code
KXJ FDA UDI
GMDN Term
Multi-purpose diagnostic imaging table FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 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

Yes

FDA UDI

Category: Multi-purpose diagnostic imaging table

Allegro Imaging Table 120V, 60HZ by Mizuho Orthopedic Systems, Inc. — Class II — 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 7217e015-aeba-4e97-8b38-cafedf3261bd 36 fields · synced Jun 9, 2026