BD Angiocath Autoguard 381705

GUDID 50382903817059

ANGIOCATH AUTOGUARD GN 18GA X 1.16IN

BECTON, DICKINSON AND COMPANY

Peripheral vascular catheter

• Primary Device ID: 50382903817059
• NIH Device Record Key: 2d5d7657-a1d5-45d5-8072-07202724c02b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Angiocath Autoguard
• Version Model Number: 381705
• Catalog Number: 381705
• Company DUNS: 124987988
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 50
• DM Exempt: true
• 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

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
• 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
• 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	00382903817054 [Unit of Use]
GS1	30382903817055 [Primary]
GS1	50382903817059 [Package]; Contains: 30382903817055; Package: Case [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201075
• Premarket Notification: K952861

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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-16

On-Brand Devices [BD Angiocath Autoguard]

• 50382903817097: ANGIOCATH AUTOGUARD ORN 14GA X 1.75IN
• 50382903817080: ANGIOCATH AUTOGUARD GRAY 16GA X 1.77IN
• 50382903817073: ANGIOCATH AUTOGUARD GRAY 16GA X 1.16IN
• 50382903817066: ANGIOCATH AUTOGUARD GN 18GA X 1.88IN
• 50382903817059: ANGIOCATH AUTOGUARD GN 18GA X 1.16IN
• 50382903817042: ANGIOCATH AUTOGUARD PNK 20GA X 1.88IN
• 50382903817035: ANGIOCATH AUTOGUARD PNK 20GA X 1.16IN
• 50382903817028: ANGIOCATH AUTOGUARD PNK 20GA X 1.0IN
• 50382903817011: ANGIOCATH AUTOGUARD BLU 22GA X 1.0IN
• 50382903817004: ANGIOCATH AUTOGUARD YEL 24GA X .75IN