SeaSpine Surgical Illuminator Cable 91-8408

GUDID 00812432020675

LUMITEX, INC.

Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable Fibreoptic light cable
Primary Device ID00812432020675
NIH Device Record Key8c006e8e-564a-4279-aa53-a0d8ae279a17
Commercial Distribution StatusIn Commercial Distribution
Brand NameSeaSpine Surgical Illuminator Cable
Version Model Number008329
Catalog Number91-8408
Company DUNS108631797
Company NameLUMITEX, INC.
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 Batchtrue
Serial Numberfalse
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
GS100812432020675 [Primary]

FDA Product Code

FDGRetractor, Fiberoptic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-08
Device Publish Date2022-07-29

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