FDA.reportPublic FDA data

CONMED

Primary DI
20653405010262
Brand
CONMED
Company
Conmed Corporation
Model
60-5181-103
Catalog number
60-5181-103
Device description
ELECTROSURGICAL ACCESSORY, Ball Electrode, 5 mm, Extended Shaft
Published
2016-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HGIELECTROCAUTERY, GYNECOLOGIC (AND ACCESSORIES)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HGIElectrocautery, Gynecologic (And Accessories)Obstetrics/Gynecology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K913213000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K913213000SINGLE USE LEE ELECTRODEAspen Laboratories, Inc.1992-02-13HGI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20653405010262PackageGS15In Commercial Distribution
10653405010265PrimaryGS10
00653405010268Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2065340501026220653405010262
1065340501026510653405010265
00653405010268006534050102686534050102680653405010268

GMDN Terms#

Term, Definition table
TermDefinition
Open-surgery electrosurgical electrode, monopolar, single-useAn invasive, monopolar, electrical conductor intended to be attached to an appropriate handle/handpiece (not included) to deliver electrosurgical current directly to tissues for cutting/coagulation during an open surgical procedure. It may be available in a variety of forms (e.g., blade, ball, loop, needle, spatula) and requires a patient contact return electrode to complete the circuit. This is a single-use device intended to be used in a sterile condition.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Outer Diameter5Millimeter

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Humidity5 Percent (%) Relative Humidity70 Percent (%) Relative Humidity
Storage Environment Temperature10 Degrees Celsius32 Degrees Celsius
Storage Environment Temperature50 Degrees Fahrenheit90 Degrees Fahrenheit

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(866)426-6633CustomerExperience@conmed.com

Regulatory Flags#

DUNS number
071595540
Device count
5
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10845854061718LASEADAPTLA3010EY10LA3010EY102020-06-01
20653405014147CONMED7-809-47-809-42016-09-24
20653405014154CONMED7-809-57-809-52016-09-24
20653405014178CONMED7-809-77-809-72016-09-24
20845854081584VIROSAFEVSOH002VSOH0022020-06-27
30653405061582DetachaTip3-10093-10092016-09-24
30653405061766DetachaTipIII3-43183-43182016-09-24
20845854649975ParadigmPRBSPRBS2022-02-08
20845854649982ParadigmPRBHPRBH2022-02-08
20845854655501Argo KnotlessKBC475-KITKBC475-KIT2026-09-25
20845854655518Argo KnotlessK475-KITK475-KIT2026-09-25
30845854655478ConMed AirsealSHELF-ICARTSHELF-ICART2026-09-18
20845854082482ParadigmPEZS01APEZS01A2020-11-16
20845854015466SEQUENTMR007CMR007C2015-10-24
20845854036584SEQUENTMR004CMR004C2015-10-24
10653405044703CORE DYNAMICSCD1406CD14062026-03-23
10653405045083CORE DYNAMICSCD1608FHCD1608FH2026-03-24
20653405990908GENESYS™ CrossFT™CFBC-4502RCFBC-4502R2026-07-31
20653405990915GENESYS™ CrossFT™CFBC-4503RCFBC-4503R2026-07-31
20653405990922GENESYS™ CrossFT™CFBC-5502RCFBC-5502R2026-07-31

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
10840113234407BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113234414BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236838BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236845BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236876BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236883BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236906BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236920BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236944BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236951BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236968BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236975BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236982BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113236999BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237002BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237019BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237026BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237033BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237057BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237071BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237095BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237125BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237149BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237156BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237163BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237170BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237187BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237194BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237200BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21
10840113237217BovieASPEN SURGICAL PRODUCTS, INC.HGI2026-09-21