GUDID 00643169352643

HOSE 1035H WAGD 5.5MM 40FT PURPLE ROHS

MEDTRONIC, INC.

Vacuum tubing, reusable

• Primary Device ID: 00643169352643
• NIH Device Record Key: b2ab6ed8-26fb-42ea-8ffe-dc180dc9d706
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 1035H
• Company DUNS: 006261481
• Company Name: MEDTRONIC, 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: false
• 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

Device Dimensions

• Length: 40 Feet
• Length: 40 Feet

Operating and Storage Conditions

• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
• Handling Environment Temperature: Between -31 Degrees Fahrenheit and 136 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169352643 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P020045

FDA Product Code

• LPB: Cardiac ablation percutaneous catheter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-05-19

Devices Manufactured by MEDTRONIC, INC.

• 00199150037667 - NA: 2025-08-11 CUSTOM PACK BB6R59R4 CP PRIME
• 00199150038756 - NA: 2025-08-11 CUSTOM PACK BB7X89R13 3/8 LOOP
• 00199150038763 - NA: 2025-08-11 CUSTOM PACK BB11Y86R6 3/8 ADULT
• 20199150038781 - NA: 2025-08-11 CUSTOM PACK BB6J25R1 10PK 3/8 TUB
• 20199150038910 - NA: 2025-08-11 CUSTOM PACK BB5S68R5 2PK RIDEOUT
• 00199150038947 - NA: 2025-08-11 CUSTOM PACK BB5P55R5 ADULT VAS
• 20199150039238 - NA: 2025-08-11 CUSTOM PACK BB12R35R 20PK ACC CON1/2X3/8
• 00199150039241 - NA: 2025-08-11 CUSTOM PACK BB11B39R3 ADULT E PACK