CERES

GUDID 00840916161934

2.5MM RETAINING SLEEVE

SPINAL ELEMENTS

Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID00840916161934
NIH Device Record Key0f52ed59-464a-4a27-8a4d-060607d03c84
Commercial Distribution StatusIn Commercial Distribution
Brand NameCERES
Version Model Number30-1024
Company DUNS004022104
Company NameSPINAL ELEMENTS
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 Usetrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100840916161934 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


[00840916161934]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-02
Device Publish Date2021-06-24

On-Brand Devices [CERES]

00840916134044Ceres Self Drilling Fixed Screw 4.0x20mm
00840916128012Ceres Self Tapping Variable Screw 4.0 x 20mm
00840916128005Ceres Self Tapping Variable Screw 4.0 x 18mm
00840916127992Ceres Self Tapping Variable Screw 4.0 x 16mm
00840916103927Ceres Self Drilling Fixed Screw 4.0x18mm
00840916102999Ceres Self Drilling Fixed Screw 4.0 x 16mm
00840916102982Ceres Self Drilling Fixed Screw 4.0 x 14mm
00840916102135Ceres Self Drilling Fixed Screw 4.0 x 12mm
00840916128050Ceres Self Tapping Variable Screw 5.0 x18mm
00840916128043Ceres Self Tapping Variable Screw 5.0 x16mm
00840916128036Ceres Self Tapping Variable Screw 5.0 x14mm
00840916128029Ceres Self Tapping Variable Screw 5.0 x12mm
00840916127985Ceres Self Tapping Variable Screw 4.0x14mm
00840916127978Ceres Self Tapping Variable Screw 4.0x12mm
00840916127961Ceres Self Tapping Fixed Screw 4.0x20mm
00840916127954Ceres Self Tapping Fixed Screw 4.0x18mm
00840916127947Ceres Self Tapping Fixed Screw 4.0x16mm
00840916127930Ceres Self Tapping Fixed Screw 4.0x14mm
00840916127923Ceres Self Tapping Fixed Screw 4.0x12mm
00840916127916Ceres Self Drilling Variable Screw 5.0 x18mm
00840916127909Ceres Self Drilling Variable Screw 5.0 x16mm
00840916127893Ceres Self Drilling Variable Screw 5.0 x14mm
00840916127886Ceres Self Drilling Variable Screw 5.0 x12mm
00840916127879Ceres Self Drilling Variable Screw 4.5 x18mm
00840916127862Ceres Self Drilling Variable Screw 4.5 x16mm
00840916127855Ceres Self Drilling Variable Screw 4.5 x14mm
00840916127848Ceres Self Drilling Variable Screw 4.5 x12mm
00840916127831Ceres Self Drilling Variable Screw 4.5 x 20mm
00840916127824Ceres self Drilling Variable Screw 4.0x20mm
00840916127817Ceres Self Drilling Variable Screw 4.0x18mm
00840916127800Ceres Self Drilling Variable Screw 4.0x16mm
00840916127794Ceres Self Drilling Variable Screw 4.0x14mm
00840916127787Ceres Self Drilling Variable Screw 4.0mmx12mm
00840916127770Ceres Rescue Variable Screw 4.5 x20mm
00840916127763Ceres Rescue Variable Screw 4.5 x18mm
00840916127756Ceres Rescue Variable Screw 4.5 x16mm
00840916127749Ceres Rescue Variable Screw 4.5 x14mm
00840916127732Ceres Rescue Variable Screw 4.5 x12mm
00840916127725Ceres Rescue Fixed Screw 4.5 x20mm
00840916127718Ceres Rescue Fixed Screw 4.5 x18mm
00840916127701Ceres Rescue Fixed Screw 4.5 x16mm
00840916127695Ceres Rescue Fixed Screw 4.5 x14mm
00840916127688Ceres Rescue Fixed Screw 4.5 x12mm
00840916127671Ceres 2-Level Midline Plate 46
00840916127664Ceres 2-Level Midline Plate 43
00840916127657Ceres 2-Level Midline Plate 40
00840916127640Ceres 2-Level Midline Plate 37
00840916127633Ceres 2-Level Midline Plate 35
00840916127626Ceres 2-Level Midline Plate 34
00840916127619Ceres 2-Level Midline Plate 32

Trademark Results [CERES]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CERES
CERES
98386800 not registered Live/Pending
Mafla Florez, Cindy Carolina
2024-02-01
CERES
CERES
98261812 not registered Live/Pending
Ceres Chill Co.
2023-11-08
CERES
CERES
98071133 not registered Live/Pending
CERES Patent & Technology, LLC
2023-07-05
CERES
CERES
98050281 not registered Live/Pending
Multiplan, Inc.
2023-06-20
CERES
CERES
97360456 not registered Live/Pending
LIYANG GLOBAL LTD.
2022-04-13
CERES
CERES
90658101 not registered Live/Pending
Vlahi Systems LLC
2021-04-20
CERES
CERES
90622304 not registered Live/Pending
UNITED FUEL SOLUTIONS LLC
2021-04-03
CERES
CERES
90609441 not registered Live/Pending
Ceres Fruit Juices (Pty) Limited
2021-03-29
CERES
CERES
88940659 not registered Live/Pending
CERES SPORT
2020-05-30
CERES
CERES
88826902 not registered Live/Pending
Ceres Intellectual Property Company Limited
2020-03-09
CERES
CERES
88702883 not registered Live/Pending
Vicostone Joint Stock Company
2019-11-22
CERES
CERES
88632024 not registered Live/Pending
Ceres
2019-09-26

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