S250 Series(Ceiling, Mobile)

GUDID 08800053093651

AC 100-240V, 50/60HZ, 61-94VA

DENTIS CO. ,LTD

Operating room light system
Primary Device ID08800053093651
NIH Device Record Key1a2c7ff9-571b-4ce0-be06-3f96ee66fb5b
Commercial Distribution StatusIn Commercial Distribution
Brand NameS250 Series(Ceiling, Mobile)
Version Model NumberS250-21000
Company DUNS694721181
Company NameDENTIS CO. ,LTD
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800053093651 [Primary]

FDA Product Code

FTDLamp, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-06
Device Publish Date2024-10-29

On-Brand Devices [S250 Series(Ceiling, Mobile)]

08800053093750AC 100-240V, 50/60HZ, 61-94VA
08800053093736AC 100-240V, 50/60HZ, 61-94VA
08800053093729AC 100-240V, 50/60HZ, 61-94VA
08800053093712AC 100-240V, 50/60HZ, 61-94VA
08800053093705AC 100-240V, 50/60HZ, 61-94VA
08800053093682AC 100-240V, 50/60HZ, 61-94VA
08800053093675AC 100-240V, 50/60HZ, 61-94VA
08800053093668AC 100-240V, 50/60Hz, 61-94VA
08800053093651AC 100-240V, 50/60HZ, 61-94VA
08800053093743AC 100-240V, 50/60HZ, 61-94VA

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