Anaesthesia screen 90321

GUDID 07640143932610

Schaerer Medical AG

Anaesthesia screen
Primary Device ID07640143932610
NIH Device Record Keyef0026ba-20b2-4590-9562-8dd9468922d0
Commercial Distribution StatusIn Commercial Distribution
Brand NameAnaesthesia screen
Version Model Numberrigid
Catalog Number90321
Company DUNS484713792
Company NameSchaerer Medical AG
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107640143932610 [Primary]

FDA Product Code

GDCTable, Operating-Room, Electrical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-05-16
Device Publish Date2025-05-08

Devices Manufactured by Schaerer Medical AG

07640143930005 - Axis2025-05-16 with side rail, without head and leg plate, with pad
07640143930012 - Axis2025-05-16 with side rail, without head and leg plate, with pad
07640143930135 - Carbon-fibre plate2025-05-16 for Axis 500 (instead seat plate)
07640143930173 - Carbon fibre-plate2025-05-16 for Axis 500/600 (instead leg plate)
07640143930654 - Carbon-fibre plate2025-05-16 for Axis
07640143930906 - Radial setting clamp2025-05-16 rotating
07640143932450 - Infusion Pole2025-05-16
07640143932610 - Anaesthesia screen2025-05-16
07640143932610 - Anaesthesia screen2025-05-16

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.