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Radiolucent Imaging Top (500#), Refurb

FDA UDI

Class I (US FDA UDI)

by Mizuho Orthopedic Systems, Inc.

Identity

Trade Name
RADIOLUCENT IMAGING TOP (500#),REFURB FDA UDI
Generic Name
Universal operating table top FDA UDI
Model / Reference
5927R FDA UDI

Identifiers

Catalog Number
5927R FDA UDI
Primary DI / UDI-DI
00842430102400 FDA UDI
FDA Product Code
JEA FDA UDI
GMDN Term
Universal operating table top 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

Yes

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: Universal operating table top

Radiolucent Imaging Top (500#), Refurb by Mizuho Orthopedic Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Universal operating table top.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fec19d3a-2a5e-4b07-a970-39c5d4d1d83d 35 fields · synced Jun 9, 2026