Procedure Products Adapters

GUDID B16080351

TORQUE DEVICE,.032 TO .038

PROCEDURE PRODUCTS, INC.

Torque manipulation device

• Primary Device ID: B16080351
• NIH Device Record Key: a4276cbe-70ad-40c0-94e2-1e403eeafad4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Procedure Products Adapters
• Version Model Number: 8035
• 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	B16080351 [Primary]

FDA Product Code

• DQX: Wire, Guide, Catheter

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: 2017-09-12

On-Brand Devices [Procedure Products Adapters]

• B16080751: Adapter, Lock to Male
• B16080421: Adapter, Male lock to Male lock
• B16080351: TORQUE DEVICE,.032 TO .038
• B160477221: I.V. UNIVERSAL STANDARD TUBING SPIKE