PITON™ Y-PACK

GUDID 20643169002955

Y-ADAPTER AC4003M PITON TJM 5PK

MEDTRONIC, INC.

Luer/Luer linear connector, single-use

• Primary Device ID: 20643169002955
• NIH Device Record Key: eb239f60-8c2f-42db-a71d-7f7dd4f70cc4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PITON™ Y-PACK
• Version Model Number: AC4003M
• 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: 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store accessories in a clean, cool and dark area.
• Special Storage Condition, Specify: Between 0 and 0 *Store accessories in a clean, cool and dark area.

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169002951 [Primary]
GS1	20643169002955 [Package]; Contains: 00643169002951; Package: PK [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K940063

FDA Product Code

• LIT: Catheter, angioplasty, peripheral, transluminal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-10-23
• Device Publish Date: 2016-07-04

On-Brand Devices [PITON™ Y-PACK]

• 20643169002955: Y-ADAPTER AC4003M PITON TJM 5PK
• 20643169843091: Y-ADAPTER AC4003M PITON TJM 5PK