← Back to catalogue

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
37 Inch frame for 4FVB-1 FDA UDI
Model / Reference
4A-PF37 Freedom FDA UDI
Description
37 Inch frame for 4FVB-1 FDA UDI

Identifiers

Catalog Number
4A-PF37 FDA UDI
Primary DI / UDI-DI
10841736115944 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

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

Manufacturer

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI 1896159f-9f2d-4ca2-b388-2a8c80b0db8e 35 fields · synced May 31, 2026