ExoShape 2500-10-000

GUDID 30653405987042

ExoShape Removal Tool Femoral

Conmed Corporation

Ligament reconstruction instrument set, reusable

• Primary Device ID: 30653405987042
• NIH Device Record Key: 2199feff-4bda-4de0-98a3-9580cab6c53c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ExoShape
• Version Model Number: 2500-10-000
• Catalog Number: 2500-10-000
• Company DUNS: 071595540
• Company Name: Conmed 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: false
• Manufacturing Date: true
• 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

Customer Support Contacts

• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing Agency	Device ID
GS1	30653405987042 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-06-10
• Device Publish Date: 2022-06-02

On-Brand Devices [ExoShape]

• 20845854082161: EXOSHAPE SOFT TISSUE FASTENER FEMORAL, 11MM x 21 MM
• 30845854082168: EXOSHAPE SOFT TISSUE FASTENER FEMORAL 11 MM
• 30845854082151: EXOSHAPE SOFT TISSUE FASTENER FEMORAL 10 MM
• 30845854082144: EXOSHAPE SOFT TISSUE FASTENER FEMORAL 9 MM
• 30845854082137: EXOSHAPE SOFT TISSUE FASTENER FEMORAL 8 MM
• 20653405986888: EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 12 MM x 30 MM
• 20653405986871: EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 11 MM x 30 MM
• 20653405986864: EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 10 MM x 30 MM
• 20653405986857: EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 9 MM x 30 MM
• 20653405986840: EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 8 MM x 30 MM
• 20653405986833: EXOSHAPE SOFT TISSUE FASTENER TIBIAL, 7 MM x 30 MM
• 30653405987141: ExoShape Sheath Inserter 10 mm
• 30653405987042: ExoShape Removal Tool Femoral
• 30653405987035: ExoShape Instrument Caddy
• 10653405987024: ExoShape Gun Tibial
• 30653405987011: ExoShape Removal Tool Tibial
• 30653405987004: ExoShape Graft Bar
• 30653405986991: ExoShape Sheath Inserter 12 mm
• 30653405986984: ExoShape Sheath Inserter 11 mm
• 10653405986973: ExoShape Sheath Inserter 9 mm
• 10653405986966: ExoShape Sheath Inserter 8 mm
• 10653405986959: ExoShape Sheath Inserter 7 mm
• 30653405986946: ExoShape Trialator 11 mm
• 30653405986939: ExoShape Trialator 10 mm
• 10653405986928: ExoShape Trialator 9 mm
• 30653405986915: ExoShape Trialator 8 mm
• 30653405986908: ExoShape Trialator 7 mm
• 10653405986898: ExoShape Trialator 6 mm