Kit, Berchtold Anesthesia Armboard OZ 7547675

GUDID 00810105030259

Radiolucent carbon fiber construction Armboard designed to integrate with surgical table side rail and support the patient arm for surgical procedures.

COMPOSITE MANUFACTURING, INC.

Arm procedure positioner, reusable

• Primary Device ID: 00810105030259
• NIH Device Record Key: 49dcb9e2-45e3-43bf-9824-93ee7baaa8ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kit, Berchtold Anesthesia Armboard
• Version Model Number: 3-2002-001
• Catalog Number: OZ 7547675
• Company DUNS: 947090650
• Company Name: COMPOSITE MANUFACTURING, INC.
• 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: 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com
• Phone: 9493617580
• Email: bmccarron@carbonfiber.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810105030259 [Primary]

FDA Product Code

• BWN: Table And Attachments, Operating-Room

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: 2021-06-22
• Device Publish Date: 2021-06-14

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