AKRUS

GUDID 04260647943573

AKRUS GmbH & Co. KG

Ophthalmic operating table, electromechanical
Primary Device ID04260647943573
NIH Device Record Key771eedfc-d423-4497-9fdd-fabe9cb52475
Commercial Distribution StatusIn Commercial Distribution
Brand NameAKRUS
Version Model NumberPatient Support System LSCneo
Company DUNS324099522
Company NameAKRUS GmbH & Co. KG
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104260647943573 [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 Date2023-12-12
Device Publish Date2023-12-04

On-Brand Devices [AKRUS]

04260647940008CZM IT760.i
04260647946239AK 106
04260647943573Patient Support System LSCneo
04260647941562SC 5010SEK
04260647941517AK 5010MBS
04260647940015CZM IT1060.i
04260647946352AK480
04260647945744AK 447
04260647945706AK446
04260647945560Doctor Stool ak 445
04260647945539Doctor stool ak 445
04260647945515AK 445

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.