H93891

GUDID 50085412476860

Vial Adapter 20mm - Luer Lock

BAXTER CORPORATION ENGLEWOOD

Vial/bottle adaptor, non-hermetic

• Primary Device ID: 50085412476860
• NIH Device Record Key: b3878909-f265-4f75-adf5-45c750608b4c
• Commercial Distribution Discontinuation: 2016-09-25
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: H93891
• Catalog Number: H93891
• Company DUNS: 078383477
• Company Name: BAXTER CORPORATION ENGLEWOOD
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com
• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com

Device Dimensions

• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter
• Lumen/Inner Diameter: 20 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00085412476865 [Primary]
GS1	50085412476860 [Package]; Contains: 00085412476865; Package: CASE [50 Units]; Discontinued: 2016-09-25; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K900585

FDA Product Code

• LHI: Set, i.V. Fluid transfer

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-07-22
• Device Publish Date: 2016-09-23

Devices Manufactured by BAXTER CORPORATION ENGLEWOOD

• 50085412478321 - RAPIDFILL: 2019-10-23 Connector, Luer Lock-to-Luer Slip
• 50085412478369 - RAPIDFILL: 2019-10-23 Connector, Luer Lock-to-Luer Lock
• 50085412478376 - RAPIDFILL: 2019-10-23 Connector, Luer Lock-to-Luer Lock with Cap
• 50085412478390 - TWOFER: 2019-08-09 TWOFER Huber-Tipped Needle
• 50085412478406 - TWOFER: 2019-08-09 TWOFER Huber-Tipped Needle
• 50085412478413 - TWOFER: 2019-08-09 TWOFER Huber-Tipped Needle
• 20085412478429 - TWOFER: 2019-08-09 TWOFER Huber-Tipped Needle
• 50085412476860 - NA: 2019-07-22Vial Adapter 20mm - Luer Lock
• 50085412476860 - NA: 2019-07-22 Vial Adapter 20mm - Luer Lock