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Skytron

FDA UDI

Class I (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
Skytron FDA UDI
Generic Name
Operating table patient positioning set, reusable FDA UDI
Device Name
G-Series 5 Inch Side Ext. Seat Section (Right) FDA UDI
Model / Reference
3-060-09-4 FDA UDI
Description
G-Series 5 Inch Side Ext. Seat Section (Right) FDA UDI

Identifiers

Catalog Number
3-060-09-4 FDA UDI
Primary DI / UDI-DI
10841736116866 FDA UDI
FDA Product Code
FQO FDA UDI
GMDN Term
Operating table patient positioning set, reusable 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

Yes

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

Dimensions & Sizes

Size
Length — 24.8 Inch FDA UDI

Category: Operating table patient positioning set, reusable

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

Similar devices

Also classified as Operating table patient positioning set, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI 4fb7a9ef-cd25-4dc1-860d-7ab3a0d03807 37 fields · synced Jun 8, 2026