Procedure Products Adapter

GUDID B16080371

Adapter, small winged

PROCEDURE PRODUCTS, INC.

General-purpose catheter connector, sterile General-purpose catheter connector, sterile

• Primary Device ID: B16080371
• NIH Device Record Key: d2a9ec7e-81a4-492e-aaec-cadaee6546ae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Procedure Products Adapter
• Version Model Number: 8037
• 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	B16080371 [Primary]

FDA Product Code

• FPA: Set, Administration, Intravascular

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: 2018-08-09
• Device Publish Date: 2017-09-12

On-Brand Devices [Procedure Products Adapter]

• B16080371: Adapter, small winged
• B16080332: ADAPTER, FEMALE LOCK TO FEMALE LOCK