CODMAN ETHISORB 831148

GUDID 10886704042693

CODMAN ETHISORB Dura Patch Polyglactin 910/poly-p-dioxanone 40mm x 60mm

CODMAN & SHURTLEFF, INC.

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• Primary Device ID: 10886704042693
• NIH Device Record Key: b2aa4afc-df94-4c54-87a6-6297450d62eb
• Commercial Distribution Discontinuation: 2022-09-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CODMAN ETHISORB
• Version Model Number: 83-1148
• Catalog Number: 831148
• Company DUNS: 607846297
• Company Name: CODMAN & SHURTLEFF, INC.
• Device Count: 1
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)255-2500
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Device Identifiers

Device Issuing Agency	Device ID
GS1	10886704042693 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K991413

FDA Product Code

• GXQ: DURA SUBSTITUTE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-01-27
• Device Publish Date: 2015-09-20

On-Brand Devices [CODMAN ETHISORB]

• 10886704042709: CODMAN ETHISORB Dura Patch Polyglactin 910/poly-p-dioxanone 60mm x 140mm
• 10886704042693: CODMAN ETHISORB Dura Patch Polyglactin 910/poly-p-dioxanone 40mm x 60mm
• 10886704042686: CODMAN ETHISORB Dura Patch Polyglactin 910/poly-p-dioxanone 20mm x 30mm