LaparoLight LLVN15012

GUDID 30845854061361

LaparoLight Veress Needle

Conmed Corporation

Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use Spring-loaded pneumoperitoneum needle, single-use

• Primary Device ID: 30845854061361
• NIH Device Record Key: d760332e-909f-4b48-906c-81e2057a16c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LaparoLight
• Version Model Number: LLVN15012
• Catalog Number: LLVN15012
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• Device Count: 12
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• 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
• 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
• 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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

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
• 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
• 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	00845854061360 [Unit of Use]
GS1	20845854061364 [Primary]
GS1	30845854061361 [Package]; Contains: 20845854061364; Package: Box [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171139

FDA Product Code

• HIF: Insufflator, laparoscopic

Sterilization

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

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

[30845854061361]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-12-15
• Device Publish Date: 2020-12-07

On-Brand Devices [LaparoLight]

• 30845854061361: LaparoLight Veress Needle
• 30845854061347: LaparoLight Veress Needle