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Assembly, Table, Proaxis, 230v

FDA UDI

Class I (US FDA UDI)

by Mizuho Orthopedic Systems, Inc.

Identity

Trade Name
ASSEMBLY, TABLE, PROAXIS, 230V FDA UDI
Generic Name
Orthopaedic operating table, electromechanical FDA UDI
Model / Reference
6988-3016I FDA UDI

Identifiers

Catalog Number
6988-3016I FDA UDI
Primary DI / UDI-DI
00842430115028 FDA UDI
FDA Product Code
JEA FDA UDI
GMDN Term
Orthopaedic operating table, electromechanical 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

Yes

FDA UDI

Category: Orthopaedic operating table, electromechanical

Assembly, Table, Proaxis, 230v by Mizuho Orthopedic Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic operating table, electromechanical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fd15e29c-90f0-40ee-a877-c20532be4f2c 34 fields · synced Jun 9, 2026