Angios Classic Angiographic Convenience Kit ANG4-0238

GUDID 00885672101879

Angiographic Convenience Kit, 4F

Oscor Inc.

Angiographic catheter, single-use Angiographic catheter, single-use

• Primary Device ID: 00885672101879
• NIH Device Record Key: d12769d0-e9f2-4e2e-ad40-51c28e4b618f
• Commercial Distribution Discontinuation: 2018-05-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Angios Classic Angiographic Convenience Kit
• Version Model Number: ANG4-0238
• Catalog Number: ANG4-0238
• Company DUNS: 101835833
• Company Name: Oscor 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: 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: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Storage Environment Temperature: Between 5 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 5 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885672101879 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092118

FDA Product Code

• DQO: CATHETER, INTRAVASCULAR, DIAGNOSTIC

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: 2018-07-06
• Device Publish Date: 2017-11-16

On-Brand Devices [Angios Classic Angiographic Convenience Kit]

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• 00885672101886: Angiographic Convenience Kit, 5F
• 00885672101879: Angiographic Convenience Kit, 4F
• 00885672101862: Angiographic Convenience Kit, 4F
• 00885672101855: Angiographic Convenience Kit, 4F
• 00885672101848: Angiographic Convenience Kit, 4F
• 00885672101817: Angiographic Convenience Kit, 6F
• 00885672101510: Angiographic Convenience Kit, 6F
• 00885672101480: Angiographic Convenience Kit, 6F
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