← Back to catalogue

Hercules

FDA UDI

Class I (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
Hercules FDA UDI
Generic Name
Universal operating table, electromechanical FDA UDI
Device Name
Battery/line powered electro-hydraulic table with removable leg and back sections and 210° table top rotation FDA UDI
Model / Reference
6702 FDA UDI
Description
Battery/line powered electro-hydraulic table with removable leg and back sections and 210° table top rotation FDA UDI

Identifiers

Primary DI / UDI-DI
10841736112196 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

Hercules 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 762fa74c-9cfa-4ed4-99bb-72cdfb466078 35 fields · synced Jun 8, 2026