← Back to catalogue

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
UltraSlide Extra Height FDA UDI
Model / Reference
3603H FDA UDI
Description
UltraSlide Extra Height FDA UDI

Identifiers

Catalog Number
3603H FDA UDI
Primary DI / UDI-DI
10841736115784 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

Yes

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI b05b7ff8-de4b-46af-b0a9-d13b61725491 36 fields · synced Jun 8, 2026