NIM CONTACT®

GUDID 00643169789562

EMG TUBE 8229507 NIM CONT 7MM ROHS

MEDTRONIC XOMED, INC.

Basic endotracheal tube, single-use

• Primary Device ID: 00643169789562
• NIH Device Record Key: 890ec323-baa4-46ae-ac66-801f7b827162
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NIM CONTACT®
• Version Model Number: 8229507
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: false
• 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(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Lumen/Inner Diameter: 7 Millimeter
• Lumen/Inner Diameter: 7 Millimeter
• Lumen/Inner Diameter: 7 Millimeter
• Lumen/Inner Diameter: 7 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169789562 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K050162

FDA Product Code

• ETN: STIMULATOR, NERVE

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: 2018-07-06
• Device Publish Date: 2016-11-06

On-Brand Devices [NIM CONTACT®]

• 00643169789579: EMG TUBE 8229508 NIM CONT 8MM ROHS
• 00643169789562: EMG TUBE 8229507 NIM CONT 7MM ROHS
• 00643169789555: EMG TUBE 8229506 NIM CONT 6MM ROHS
• 00643169358775: ENDOTRACH TUBE 8229508 CONT EMG 8MM ROHS
• 00643169358768: ENDOTRACH TUBE 8229507 CONT EMG 7MM ROHS
• 00643169358751: ENDOTRACH TUBE 8229506 CONT EMG 6MM ROHS