Lumbar Interbody Fusion System (OLLIF) Instrument Set in Sterilization Case 01-2001

GUDID 00850014575038

Lumbar Interbody Fusion System (OLLIF) Instrument Set in Sterilization Case

ADVANCED RESEARCH MEDICAL LLC

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Primary Device ID00850014575038
NIH Device Record Keye7c44ba9-b63a-419b-9c4c-a55907e4e363
Commercial Distribution StatusIn Commercial Distribution
Brand NameLumbar Interbody Fusion System (OLLIF) Instrument Set in Sterilization Case
Version Model Number01-2001
Catalog Number01-2001
Company DUNS117201206
Company NameADVANCED RESEARCH MEDICAL LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com
Phone(612)440-1865
Emailinfo@advresmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850014575038 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


[00850014575038]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-12-24
Device Publish Date2019-12-16

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00840239800657 - N/A2024-04-29 XL-Graft Tamp
00840239800671 - N/A2024-04-29 XL-Flexible Curette - Outer
00840239800527 - N/A2024-04-26 XL-Articulating Curette
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00840239800510 - N/A2024-04-24 XL-Shaper - Blades

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