MaxGuard, MaxPlus MP9230

GUDID 10885403237065

7-IN STANDARDBORE TRI-FUSE SET

BD Switzerland Sàrl

Intravenous administration tubing extension set

• Primary Device ID: 10885403237065
• NIH Device Record Key: 3497dcc1-131e-4b59-91aa-b022a782859f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MaxGuard, MaxPlus
• Version Model Number: MP9230
• Catalog Number: MP9230
• Company DUNS: 482631558
• Company Name: BD Switzerland Sàrl
• 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: 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(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com
• Phone: +1(844)823-5433
• Email: customer_support@bd.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885403237065 [Primary]
GS1	50885403237063 [Package]; Package: Case [50 Units]; In Commercial Distribution

FDA Product Code

• FPA: Set, administration, intravascular

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: 2024-08-14
• Device Publish Date: 2016-09-22

On-Brand Devices [MaxGuard, MaxPlus]

• 10885403237089: Tri-fuse extension set, (minibore) 3 clear needleless connector 18 cm (7 in)
• 10885403237003: Tri-Fuse extension set, (minibore) with 3 removeable clear needleless connectors 18 cm (7 in)
• 10885403274541: 36 IN MINIBORE TRI-FUSE SET
• 10885403236846: 8-IN MINIBORE BI-FUSE SET
• 10885403274565: 9-IN MINIBORE TRI-FUSE SET
• 10885403237065: 7-IN STANDARDBORE TRI-FUSE SET