SOLED15-F 110402

GUDID 08050705890316

SOLED15-F WALL

ACEM SPA

Fixed examination/treatment light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light
Primary Device ID08050705890316
NIH Device Record Keydac0c0d6-cca7-4f4a-ac12-213a681a6e73
Commercial Distribution StatusIn Commercial Distribution
Brand NameSOLED15-F
Version Model NumberSOLED15-F /W
Catalog Number110402
Company DUNS435188508
Company NameACEM SPA
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
GS108050705890316 [Primary]

FDA Product Code

KZFDevice, Medical Examination, Ac Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-03-20
Device Publish Date2020-01-31

On-Brand Devices [SOLED15-F]

08050705890354SOLED15-F 2-ARM CEILING STANDARD LINE
08050705890347SOLED15-F 1-ARM CEILING STANDARD LINE
08050705890330SOLED15-F TROLLEY ABPS
08050705890323SOLED15-F TROLLEY
08050705890316SOLED15-F WALL
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