Procedure Products Needles

GUDID B160211827P1

18 GA needle, 7cm, BSDN, with Plug

PROCEDURE PRODUCTS, INC.

Vascular catheter introduction needle Vascular catheter introduction needle

• Primary Device ID: B160211827P1
• NIH Device Record Key: 80390fb5-534a-4496-98eb-767b78ea7f03
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Procedure Products Needles
• Version Model Number: 21-1827-P
• Company DUNS: 151507563
• Company Name: PROCEDURE PRODUCTS, INC.
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B160211827P1 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K810859

FDA Product Code

• DRE: Dilator, Vessel, For Percutaneous Catheterization

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: 2017-09-27

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