SPECTRUM AUTOPASS SMI-02AP

GUDID 10845854042243

SPECTRUM AUTOPASS SUTURE PASSER

Conmed Corporation

Suturing needle, single-use Suturing needle, single-use Suturing needle, single-use Suturing needle, single-use Suturing needle, single-use Suturing needle, single-use Suturing needle, single-use Suturing needle, single-use Suturing needle, single-use

• Primary Device ID: 10845854042243
• NIH Device Record Key: 23e9b58d-e26e-4a68-b280-5dc2f5cd92dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SPECTRUM AUTOPASS
• Version Model Number: SMI-02AP
• Catalog Number: SMI-02AP
• 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: true
• Lot Batch: false
• Serial Number: true
• 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
• 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
• 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	10845854042243 [Primary]
GS1	20845854042240 [Direct Marking]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-07-25
• Device Publish Date: 2021-05-30

Devices Manufactured by Conmed Corporation

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• 30653405988681 - Argo Knotless GENESYS: 2024-04-22 4.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, Blue/Blue
• 30653405988698 - Argo Knotless GENESYS: 2024-04-22 4.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, White/Black
• 30653405988735 - Argo Knotless GENESYS: 2024-04-22 5.5 mm Argo KnotlessTM GENESYSTM Disposable Tap
• 30653405988742 - Argo Knotless GENESYS: 2024-04-22 4.75 mm Argo KnotlessTM GENESYSTM Disposable Tap