NuMED, Inc. Bonhoeffer RM0279-01

GUDID 0887714024532

LAKE REGION MEDICAL LIMITED

Peripheral vascular guidewire, manual

• Primary Device ID: 0887714024532
• NIH Device Record Key: c7400de2-7235-4d1c-a7a3-1f636955f1e3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NuMED, Inc. Bonhoeffer
• Version Model Number: J3FC-SS C 210-035
• Catalog Number: RM0279-01
• Company DUNS: 988555595
• Company Name: LAKE REGION MEDICAL LIMITED
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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

Customer Support Contacts

• Phone: (315) 328-4491
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	0887714024532 [Package]; Contains: 10887714024532; Package: Single Pack Sterile [5 Units]; In Commercial Distribution
GS1	10887714024532 [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: 2016-10-11

On-Brand Devices [NuMED, Inc. Bonhoeffer]

• 0887714024532: J3FC-SS C 210-035
• 10887714030380: J3FC-SS C 210-035