InfuseIT ZIT-502

GUDID 10607411913409

InfuseIT 500 ml Disposable Pressure Infusor

SALTER LABS

Intravenous pressure infusor, manual

• Primary Device ID: 10607411913409
• NIH Device Record Key: d42e2950-9e7a-4e2a-bcaf-fe41d91fffc4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: InfuseIT
• Version Model Number: ZIT-502
• Catalog Number: ZIT-502
• Company DUNS: 022721133
• Company Name: SALTER LABS
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)421-0024
• Email: customercare@salterlabs.com
• Phone: +1(800)421-0024
• Email: customercare@salterlabs.com
• Phone: +1(800)421-0024
• Email: customercare@salterlabs.com

Device Dimensions

• Total Volume: 500 Milliliter
• Total Volume: 500 Milliliter
• Total Volume: 500 Milliliter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607411913402 [Primary]
GS1	10607411913409 [Package]; Contains: 00607411913402; Package: [10 Units]; In Commercial Distribution
GS1	20607411913406 [Package]; Package: [8 Units]; In Commercial Distribution

FDA Product Code

• KZD: INFUSOR, PRESSURE, FOR I.V. BAGS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

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