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Skytron

FDA UDI

Class I (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
Skytron FDA UDI
Generic Name
General utility supply system, ceiling-mounted FDA UDI
Device Name
Handle, single for 4FVB-1/2 FDA UDI
Model / Reference
4A-FHA Freedom FDA UDI
Description
Handle, single for 4FVB-1/2 FDA UDI

Identifiers

Catalog Number
4A-FHA FDA UDI
Primary DI / UDI-DI
10841736115920 FDA UDI
FDA Product Code
FQO FDA UDI
GMDN Term
General utility supply system, ceiling-mounted 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General utility supply system, ceiling-mounted

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

Similar devices

Also classified as General utility supply system, ceiling-mounted.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI 22177028-2407-40b9-9dd0-f26a069da4a5 35 fields · synced May 30, 2026