GUDID 03700712404918

EPS 20 TR

MAQUET SAS

Operating room light
Primary Device ID03700712404918
NIH Device Record Key0db71ff3-ac29-4e98-839a-602f388dcc98
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberARD567355901
Company DUNS264700139
Company NameMAQUET SAS
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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
GS103700712404918 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FTDLamp, surgical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-01-08
Device Publish Date2016-09-16

Devices Manufactured by MAQUET SAS

03700712434519 - Volista2025-02-26 VSTII40SF XHD127 SAX1216
03700712434533 - Volista2025-02-26 VCSII64DF TK SB1011
03700712414283 - Maquet Equipment2025-01-14 EQTXS3216 SAT12
03700712414290 - Maquet Equipment2025-01-14 EQTXS3216 SAT13
03700712414306 - Maquet Equipment2025-01-14 EQTXS3216 11
03700712415662 - Volista2025-01-14 VST66SF VP TK AIM 1011
03700712415693 - Volista2025-01-14 VST64DF VP TK AIM 0810
03700712432713 - Volista2025-01-13 VCSII64SFDF SB1011

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