Corrugated Tubing Cuttable Cuffs

GUDID 00709078013980

Corrugated Tubing Cuttable Cuffs Every 6" 22mm X 100' (Translucent)

WESTMED, INC.

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• Primary Device ID: 00709078013980
• NIH Device Record Key: 58300fe5-b36b-48ef-a609-154e04c3a876
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Corrugated Tubing Cuttable Cuffs
• Version Model Number: 1002060
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078013980 [Primary]

FDA Product Code

• BYX: Tubing, Pressure And Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-04-08
• Device Publish Date: 2022-03-31

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