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UltraSlide

FDA UDI

Class I (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
UltraSlide FDA UDI
Generic Name
Universal operating table, electromechanical FDA UDI
Device Name
ULTRA SLIDE FDA UDI
Model / Reference
3603 FDA UDI
Description
ULTRA SLIDE FDA UDI

Identifiers

Primary DI / UDI-DI
10841736112172 FDA UDI
FDA Product Code
FQO FDA UDI
GMDN Term
Universal 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Universal operating table, electromechanical

UltraSlide by Skytron, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Universal operating table, electromechanical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI f4e43376-4999-467c-9e28-d95f0c93459d 35 fields · synced Jun 8, 2026