F101 SERIES MOUNT WITH 1 LF ARM F101 Series

GUDID 10841736124304

F101 SERIES MOUNT WITH 1 LF ARM

SKYTRON LLC

General utility supply system, ceiling-mounted
Primary Device ID10841736124304
NIH Device Record Keyd2e6ef22-cca6-4a66-9730-848b4b8a9b2f
Commercial Distribution StatusIn Commercial Distribution
Brand NameF101 SERIES MOUNT WITH 1 LF ARM
Version Model NumberF101 Series
Catalog NumberF101 Series
Company DUNS078375583
Company NameSKYTRON LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us

Device Identifiers

Device Issuing AgencyDevice ID
GS110841736124304 [Primary]

FDA Product Code

FQOTable, Operating-Room, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-05-19
Device Publish Date2025-05-11

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