VENOJECT

GUDID 54987350727126

VENOJECT Multi-Sample Luer Adapter

TERUMO CORPORATION

Luer-ended blood collection tube spike

• Primary Device ID: 54987350727126
• NIH Device Record Key: 18400431-8222-4038-8d21-ae4709504f93
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VENOJECT
• Version Model Number: XX*MN2000TE
• Company DUNS: 690543319
• Company Name: TERUMO CORPORATION
• Device Count: 100
• 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: true
• 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)283-7866
• Email: tmccustomer.admin@terumomedical.com
• Phone: +1(800)283-7866
• Email: tmccustomer.admin@terumomedical.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity. Avoid direct sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity. Avoid direct sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity. Avoid direct sunlight.
• Special Storage Condition, Specify: Between 0 and 0 *Do not store at extreme temperature and humidity. Avoid direct sunlight.

Device Identifiers

Device Issuing Agency	Device ID
GS1	04987350727121 [Unit of Use]
GS1	34987350727122 [Primary]
GS1	54987350727126 [Package]; Contains: 34987350727122; Package: [30 Units]; In Commercial Distribution

FDA Product Code

• JKA: Tubes, vials, systems, serum separators, blood collection

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: 2019-10-23
• Device Publish Date: 2016-09-09

Devices Manufactured by TERUMO CORPORATION

• 54987350743256 - CAPIOX: 2024-05-28 CAPIOX CARDIOPLEGIA
• 54987350705629 - SURSHIELD: 2024-05-06 SURSHIELD-PUR SAFETY I.V.Catheter
• 54987350705667 - SURSHIELD: 2024-05-06 SURSHIELD-PUR SAFETY I.V.Catheter
• 54987350705704 - SURSHIELD: 2024-05-06 SURSHIELD-PUR SAFETY I.V.Catheter
• 54987350705728 - SURSHIELD: 2024-05-06 SURSHIELD-PUR SAFETY I.V.Catheter
• 54987350705742 - SURSHIELD: 2024-05-06 SURSHIELD-PUR SAFETY I.V.Catheter
• 54987350705766 - SURSHIELD: 2024-05-06 SURSHIELD-PUR SAFETY I.V.Catheter
• 04987350745088 - GLIDEWIRE ADVANTAGE: 2024-03-08 RADIFOCUS GLIDEWIRE ADVANTAGE Guidewire