STERLING C9248

GUDID 20845854012533

3.5MM STERLING FULL RADIUS RESECTOR

Conmed Corporation

Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use Arthroscopic shaver system blade, single-use
Primary Device ID20845854012533
NIH Device Record Key1946920d-6405-44d1-a9f8-9af08d6aa2d0
Commercial Distribution StatusIn Commercial Distribution
Brand NameSTERLING
Version Model NumberC9248
Catalog NumberC9248
Company DUNS071595540
Company NameConmed Corporation
Device Count6
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing AgencyDevice ID
GS100845854012539 [Unit of Use]
GS110845854012536 [Primary]
GS120845854012533 [Package]
Contains: 10845854012536
Package: Carton [1 Units]
In Commercial Distribution

FDA Product Code

GFABLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-10-25
Device Publish Date2021-10-15

On-Brand Devices [STERLING]

108458540205624.2MM X 19CM GATOR SHAVER, EXTENDED LENGTH
208458540180543.5MM FULL RADIUS RESECTOR, SMALL HUB
208458540180095.5MM STERLING SPHERICAL BUR, SMALL HUB, 6 EA
208458540174604.8MM FULL RADIUS RESECTOR, SMALL HUB
208458540186584.5MM X 19CM STERLING SPHERICAL BUR, EXTENDED LENGTH
208458540217192.9MM STERLING FULL RADIUS RESECTOR
208458540217022.0MM STERLING FULL RADIUS RESECTOR
208458540181532.9MM STERLING VORTEX, MICROBLADE
208458540179892.9MM STERLING, FULL RADIUS RESECTOR MICROBLADE
208458540179653.5MM STERLING, FULL RADIUS RESECTOR MICROBLADE
208458540177433.5MM STERLING VORTEX, MICROBLADE
208458540177362.0MM STERLING, FULL RADIUS RESECTOR MICROBLADE
208458540177292.9MM STERLING SPHERICAL BUR, MICROBLADE
208458540172864.2MM STERLING END CUTTER
208458540125264.8MM STERLING FULL RADIUS RESECTOR
208458540175906.0MM STERLING, OVAL BUR, SMALL HUB
208458540174394.5MM STERLING SPHERICAL BUR, SMALL HUB
208458540172174.0MM STERLING OVAL BUR
208458540181223.5MM STERLING SPHERICAL BUR, MICROBLADE
208458540175525.5MM STERLING MENISCUS CUTTER
208458540173853.5MM STERLING END CUTTER
208458540127793.5MM STERLING MENISCUS CUTTER
208458540125642.9MM STERLING SPHERICAL BUR
208458540125333.5MM STERLING FULL RADIUS RESECTOR
308458540296754.5MM STERLING, LIGHTNING
308458540296204.0MM STERLING OVAL BUR, REDUCED HOOD
308458540204674.2MM, LARGE HUB, STERLING, SHAVER, 15 DEGREE FULL-RADIUS RESECTOR
308458540177954.0MM STERLING, TAPERED BUR
308458540125926.0MM STERLING, VORTEX
308458540125854.5MM STERLING VORTEX

Trademark Results [STERLING]

Mark Image

Registration | Serial
Company
Trademark
Application Date
STERLING
STERLING
98321003 not registered Live/Pending
Brown, David S.
2023-12-19
STERLING
STERLING
98302852 not registered Live/Pending
College Park Industries, Inc.
2023-12-07
STERLING
STERLING
97836074 not registered Live/Pending
Sterling Data Company, LLC
2023-03-13
STERLING
STERLING
97727122 not registered Live/Pending
Sterling Site Access Solutions, LLC
2022-12-21
STERLING
STERLING
97710539 not registered Live/Pending
Diamond Saw Works, Inc.
2022-12-09
STERLING
STERLING
97124178 not registered Live/Pending
Hockey Town Holdings LLC
2021-11-14
STERLING
STERLING
97124070 not registered Live/Pending
Hockey Town Holdings LLC
2021-11-14
STERLING
STERLING
97021964 not registered Live/Pending
Fulton and Roark, LLC
2021-09-10
STERLING
STERLING
90898652 not registered Live/Pending
GTRC Services, Inc.
2021-08-24
STERLING
STERLING
90862468 not registered Live/Pending
Drew Layne, LLC
2021-08-03
STERLING
STERLING
90734184 not registered Live/Pending
Menahem, David
2021-05-25
STERLING
STERLING
90581533 not registered Live/Pending
Eickhof Columbaria Inc.
2021-03-16

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.