Benefix™ Interspinous Fixation System

GUDID 08800037551030

U&I CORPORATION

Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable

Primary Device ID	08800037551030
NIH Device Record Key	f46c9dcd-6ce2-4b4f-b147-dd7db089ce23
Commercial Distribution Status	In Commercial Distribution
Brand Name	Benefix™ Interspinous Fixation System
Version Model Number	ISS2030
Company DUNS	688811082
Company Name	U&I CORPORATION
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	true
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800037551030 [Primary]

FDA Product Code

FZX	Guide, surgical, instrument

Sterilization

Steralize Prior To Use	true
Device Is Sterile	false

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

[08800037551030]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2021-09-23
Device Publish Date	2021-09-15

On-Brand Devices [Benefix™ Interspinous Fixation System]

08800015921046	IS30180
08800015921039	IS30160
08800015921022	IS30140
08800015921015	IS30120
08800015921008	IS30100
08800015920995	IS30080
08800015920988	IS30060
08800015920971	IS21850R
08800015920964	IS21850L
08800015920957	IS21849R
08800015920940	IS21849L
08800015920933	IS21848R
08800015920926	IS21848L
08800015920919	IS21847R
08800015920902	IS21847L
08800015920896	IS21846R
08800015920889	IS21846L
08800015920872	IS21845R
08800015920865	IS21845L
08800015920858	IS21844R
08800015920841	IS21844L
08800015920834	IS21843R
08800015920827	IS21843L
08800015920810	IS21842R
08800015920803	IS21842L
08800015920797	IS21841R
08800015920780	IS21841L
08800015920773	IS21840R
08800015920766	IS21840L
08800015920759	IS21839R
08800015920742	IS21839L
08800015920735	IS21838R
08800015920728	IS21838L
08800015920711	IS21837R
08800015920704	IS21837L
08800015920698	IS21650R
08800015920681	IS21650L
08800015920674	IS21649R
08800015920667	IS21649L
08800015920650	IS21648R
08800015920643	IS21648L
08800015920636	IS21647R
08800015920629	IS21647L
08800015920612	IS21646R
08800015920605	IS21646L
08800015920599	IS21645R
08800015920582	IS21645L
08800015920575	IS21644R
08800015920568	IS21644L
08800015920551	IS21643R

Trademark Results [Benefix]

Mark Image Registration \| Serial	Company Trademark Application Date
BENEFIX 87367180 5410614 Live/Registered	BeneFix, LLC 2017-03-10
BENEFIX 87367107 5410613 Live/Registered	BeneFix, LLC 2017-03-10
BENEFIX 78872293 3217619 Live/Registered	SS&C TECHNOLOGIES, INC. 2006-04-28
BENEFIX 75376195 2413376 Dead/Cancelled	2900084 CANADA INC. 1997-10-20
BENEFIX 75038324 2102082 Live/Registered	GENETICS INSTITUTE, LLC 1995-12-26
BENEFIX 74377205 1814054 Dead/Cancelled	Blue Cross and Blue Shield 1993-04-09

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