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Axis

FDA UDI

Class I (US FDA UDI)

by Schaerer Medical AG

Identity

Trade Name
Axis FDA UDI
Generic Name
Universal operating table, electrohydraulic FDA UDI
Device Name
with side rail, without head and leg plate, with pad FDA UDI
Model / Reference
600 FDA UDI
Description
with side rail, without head and leg plate, with pad FDA UDI

Identifiers

Catalog Number
91596 FDA UDI
Primary DI / UDI-DI
07640143930012 FDA UDI
FDA Product Code
GDC FDA UDI
GMDN Term
Universal operating table, electrohydraulic 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: Universal operating table, electrohydraulic

Axis by Schaerer Medical AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Universal operating table, electrohydraulic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Schaerer Medical AG

Sources (1)

  • FDA UDI 2281f64e-23ad-4a21-9049-21421f77ae58 34 fields · synced May 31, 2026