Perfix™ Iliac Screw System

GUDID 08800037551023

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

Primary Device ID	08800037551023
NIH Device Record Key	7dc3fa9d-3586-4887-a7c1-ae341dfa1e5c
Commercial Distribution Status	In Commercial Distribution
Brand Name	Perfix™ Iliac Screw System
Version Model Number	SL0020
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	08800037551023 [Primary]

FDA Product Code

FZX	Guide, surgical, instrument

Sterilization

Steralize Prior To Use	true
Device Is Sterile	false

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

[08800037551023]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2021-09-24
Device Publish Date	2021-09-16

On-Brand Devices [Perfix™ Iliac Screw System]

08800015952651	SL001-E
08800015952644	SL001-D
08800015952637	SL001-C
08800015952620	SL001-B
08800015952613	SL001-A
08800015952606	SL001
08800015952590	SL0050
08800015952583	SL0040
08800015952576	SL0030
08800015952569	SL0020
08800015952552	SL0010
08800015931878	SL9590
08800015931861	SL9580
08800015931854	SL9570
08800015931847	SL9560
08800015931830	SL9550
08800015931823	SL9540
08800015931816	SL9510
08800015931809	SL8590
08800015931793	SL8580
08800015931786	SL8570
08800015931779	SL8560
08800015931762	SL8550
08800015931755	SL8540
08800015931748	SL8510
08800015931731	SL7590
08800015931724	SL7580
08800015931717	SL7570
08800015931700	SL7560
08800015931694	SL7550
08800015931687	SL7540
08800015931670	SL7510
08800015931663	SL6590
08800015931656	SL6580
08800015931649	SL6570
08800015931632	SL6560
08800015931625	SL6550
08800015931618	SL6540
08800015931601	SL6510
08800015931595	SL0226
08800015931588	SL0225
08800015931571	SL0224
08800015931564	SL0223
08800015931557	SL0222
08800015931540	SL0221
08800015931533	SL0216
08800015931526	SL0215
08800015931502	SL0213
08800015931496	SL0212
08800015931489	SL0211

Trademark Results [Perfix]

Mark Image Registration \| Serial	Company Trademark Application Date
PERFIX 90374997 not registered Live/Pending	Perfix Inc. 2020-12-11
PERFIX 85691869 4349179 Live/Registered	Atica Nails Inc. 2012-07-31
PERFIX 80985733 0985733 Dead/Cancelled	Applied Bioscience 0000-00-00
PERFIX 79005104 not registered Dead/Abandoned	Partnership Twello B.V. 2003-11-03
PERFIX 77145921 3439246 Dead/Cancelled	PERESYS (PROPRIETARY) LIMITED 2007-04-02
PERFIX 75568540 2295911 Dead/Cancelled	Affiniti L.L.C. 1998-10-13
PERFIX 74351154 1896892 Live/Registered	C.R. BARD, INC. 1993-01-22
PERFIX 74012649 1620984 Dead/Cancelled	VARIAN ASSOCIATES, INC. 1989-12-20
PERFIX 72235990 0818539 Dead/Expired	THOMAS L. KALAHAR, DOING BUSINESS AS KALAHAR & COMPANY AND PERF HOOK MANUFACTURING COMPANY 1966-01-07

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