LUMISTM

GUDID 03663136001210

LUMIS Tray 1

SPINEVISION

Instrument tray Instrument tray Instrument tray Instrument tray
Primary Device ID03663136001210
NIH Device Record Key80d62486-e4b8-4b10-9c5e-90163930e447
Commercial Distribution StatusIn Commercial Distribution
Brand NameLUMISTM
Version Model NumberMS1-TRAY111
Company DUNS390377518
Company NameSPINEVISION
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+33153332525
Emailcorp.quality@spinevision.com
Phone+33153332525
Emailcorp.quality@spinevision.com
Phone+33153332525
Emailcorp.quality@spinevision.com
Phone+33153332525
Emailcorp.quality@spinevision.com

Device Identifiers

Device Issuing AgencyDevice ID
GS103663136001210 [Primary]
GS103663136001210 [Primary]
GS103663136001210 [Primary]
GS103663136001210 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03663136001210]

Moist Heat or Steam Sterilization


[03663136001210]

Moist Heat or Steam Sterilization


[03663136001210]

Moist Heat or Steam Sterilization


[03663136001210]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-10
Device Publish Date2020-11-02

On-Brand Devices [LUMISTM]

03663136001227LUMIS Identification Plate
03663136001210LUMIS Tray 1
03663136001203LUMIS Tray 2

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