BD Angiocath 381144

GUDID 50382903811446

ANGIOCATH GN 18GA X 1.16IN

BECTON, DICKINSON AND COMPANY

Peripheral vascular catheter Peripheral vascular catheter Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula Peripheral intravenous cannula

• Primary Device ID: 50382903811446
• NIH Device Record Key: 1a04181b-1944-4ffd-b606-50da84533938
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Angiocath
• Version Model Number: 381144
• Catalog Number: 381144
• Company DUNS: 124987988
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 50
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382903811441 [Unit of Use]
GS1	30382903811442 [Primary]
GS1	50382903811446 [Package]; Contains: 30382903811442; Package: Case [4 Units]; In Commercial Distribution

FDA Product Code

• FOZ: Catheter,intravascular,therapeutic,short-term less than 30 days

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-16

On-Brand Devices [BD Angiocath]

• 50382903822879: ANGIOCATH SPECIAL TAN 10GA X 3.0IN
• 50382903822770: ANGIOCATH SPECIAL LGT BL 12GA X 3.0IN
• 50382903822695: ANGIOCATH SPECIAL ORN 14GA X 5.25IN
• 50382903822688: ANGIOCATH SPECIAL ORN 14GA X 3.25IN
• 50382903822596: ANGIOCATH SPECIAL GRAY 16GA X 5.25IN
• 50382903822589: ANGIOCATH SPECIAL GRAY 16GA X 3.25IN
• 50382903811675: ANGIOCATH ORN 14GA X 1.88IN
• 50382903811644: ANGIOCATH ORN 14GA X 1.16IN
• 50382903811576: ANGIOCATH GRAY 16GA X 1.88IN
• 50382903811545: ANGIOCATH GRAY 16GA X 1.16IN
• 50382903811477: ANGIOCATH GN 18GA X 1.88IN
• 50382903811446: ANGIOCATH GN 18GA X 1.16IN
• 50382903811378: ANGIOCATH PNK 20GA X 1.88IN
• 50382903811347: ANGIOCATH PNK 20GA X 1.16IN
• 50382903811231: ANGIOCATH BL 22GA X 1.0IN
• 50382903811125: ANGIOCATH YEL 24GA X 0.75IN