NIM FLEX™

GUDID 20643169358786

ENDOTRACH TUBE 8229960 5PK EMG 6MM ROHS

MEDTRONIC XOMED, INC.

Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use

• Primary Device ID: 20643169358786
• NIH Device Record Key: 211cb299-f18b-4cef-b43b-e4cf2eb32882
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NIM FLEX™
• Version Model Number: 8229960
• 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: false
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169358782 [Primary]
GS1	20643169358786 [Package]; Contains: 00643169358782; Package: PK [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K925640

FDA Product Code

• ETN: STIMULATOR, NERVE

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-10
• Device Publish Date: 2019-05-02

On-Brand Devices [NIM FLEX™]

• 20643169358830: ENDOTRACH TUBE 8229985 5PK EMG 8.5 ROHS
• 20643169358823: ENDOTRACH TUBE 8229980 5PK EMG 8MM ROHS
• 20643169358816: ENDOTRACH TUBE 8229975 5PK EMG 7.5 ROHS
• 20643169358809: ENDOTRACH TUBE 8229970 5PK EMG 7MM ROHS
• 20643169358793: ENDOTRACH TUBE 8229965 5PK EMG 6.5 ROHS
• 20643169358786: ENDOTRACH TUBE 8229960 5PK EMG 6MM ROHS
• 20885074446091: ENDOTRACH TUBE 8229985 5PK 8.5MM EMG FLX
• 20885074446060: ENDOTRACH TUBE 8229980 5PK 8MM EMG FLEX