ACEMSO15F 110506

GUDID 08050705890408

ACEMSO15F 2-ARM CEILING STANDARD LINE

ACEM SPA

Fixed examination/treatment light
Primary Device ID08050705890408
NIH Device Record Key2ce85ab8-d222-4959-b453-47b29808abe2
Commercial Distribution StatusIn Commercial Distribution
Brand NameACEMSO15F
Version Model NumberACEMSO15F /SC2
Catalog Number110506
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
GS108050705890408 [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 [ACEMSO15F]

08050705890408ACEMSO15F 2-ARM CEILING STANDARD LINE
08050705890392ACEMSO15F 1-ARM CEILING STANDARD LINE
08050705890385ACEMSO15F TROLLEY ABPS
08050705890378ACEMSO15F TROLLEY
08050705890361ACEMSO15F WALL

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