CLEARWAY

GUDID 00650862802320

CLEARWAY, RX 3.00X20MM

ATRIUM MEDICAL CORPORATION

Peripheral vascular infusion catheter

• Primary Device ID: 00650862802320
• NIH Device Record Key: 7c5932d2-543c-49d6-8e00-bbf89f93639a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CLEARWAY
• Version Model Number: 80232
• Company DUNS: 051798999
• Company Name: ATRIUM MEDICAL CORPORATION
• 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: false
• Serial Number: true
• 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
GS1	00650862802320 [Primary]

FDA Product Code

• DQY: CATHETER, PERCUTANEOUS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-04-09
• Device Publish Date: 2015-09-24

On-Brand Devices [CLEARWAY]

• 00650862802535: CLEARWAY, RX 4.00X50MM
• 00650862802504: CLEARWAY, RX 4.00X20MM
• 00650862802443: CLEARWAY, RX 3.50X20MM
• 00650862802351: CLEARWAY, RX 3.00X50MM
• 00650862802320: CLEARWAY, RX 3.00X20MM
• 00650862802207: CLEARWAY, RX 2.50X20MM
• 00650862802177: CLEARWAY, RX 2.00X50MM
• 00650862802146: CLEARWAY, RX 2.00X20MM
• 00650862802085: CLEARWAY, RX 1.50X20MM
• 00650862802023: CLEARWAY, RX 1.00X20MM
• 00650862802009: CLEARWAY, RX 1.00X10MM