Angios Classic Angiographic Catheter ANG1-0498

GUDID 50836559008601

Angiographic Catheter, STRAIGHT PIGTAIL, 5F, 17 mm

Oscor Inc.

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

• Primary Device ID: 50836559008601
• NIH Device Record Key: 75ec98f9-55dd-4043-bf23-2d5e6ec0f2f1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Angios Classic Angiographic Catheter
• Version Model Number: ANG1-0498
• Catalog Number: ANG1-0498
• Company DUNS: 101835833
• Company Name: Oscor Inc.
• Device Count: 100
• 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: 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
• Length: 90 Centimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 90 Centimeter
• 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	00836559008606 [Unit of Use]
GS1	50836559008601 [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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-11-16

On-Brand Devices [Angios Classic Angiographic Catheter]

• 50885672104165: Angiographic Catheter, Multipurpose A I, 6F
• 50885672104158: Angiographic Catheter, Multipurpose A I, 5F
• 50885672104141: Angiographic Catheter, Multipurpose A I, 5F
• 50885672104110: Angiographic Catheter, NIH, 6F
• 50885672104103: Angiographic Catheter, NIH, 5F
• 50885672104097: Angiographic Catheter, NIH, 5F
• 50885672104042: Angiographic Catheter, Internal Mammary, 5F
• 50885672104011: Angiographic Catheter, Amplatz Left II, 6F
• 50885672104004: Angiographic Catheter, Amplatz Left II, 5F
• 50885672103991: Angiographic Catheter, Amplatz Left II, 5F
• 50885672103960: Angiographic Catheter, Amplatz Left I, 5F
• 50885672103953: Angiographic Catheter, Amplatz Left I, 5F
• 50885672103878: Angiographic Catheter, Amplatz Right I Mod, 6F
• 50885672103861: Angiographic Catheter, Amplatz Right I Mod, 5F
• 50885672103854: Angiographic Catheter, Amplatz Right I Mod, 5F
• 50885672103755: Angiographic Catheter, JR 3.5, 5F
• 50885672103748: Angiographic Catheter, JL 3.5, 5F
• 50885672103700: Angiographic Catheter, JR 3.0, 6F
• 50885672103694: Angiographic Catheter, JL 3.0, 6F
• 50885672103656: Angiographic Catheter, JR 6.0, 6F
• 50885672103649: Angiographic Catheter, JL 6.0, 6F
• 50885672103632: Angiographic Catheter, JR 5.0, 6F
• 50885672103625: Angiographic Catheter, JL 5.0, 6F
• 50885672103618: Angiographic Catheter, JR 4.5, 6F
• 50885672103601: Angiographic Catheter, JL 4.5, 6F
• 50885672103595: Angiographic Catheter, JR 3.5, 6F
• 50885672103588: Angiographic Catheter, JL 3.5, 6F
• 50885672102994: Angiographic Catheter, Internal Mammary, 6F
• 50885672102987: Angiographic Catheter, Amplatz Left II, 6F
• 50885672102970: Angiographic Catheter, Amplatz Left I, 6F
• 50885672102963: Angiographic Catheter, Amplatz Right II Mod, 6F
• 50885672102956: Angiographic Catheter, Amplatz Right I Mod, 6F
• 50885672102949: Angiographic Catheter, Multipurpose A I, 6F
• 50885672102925: Angiographic Catheter, NIH, 6F
• 50885672102918: Angiographic Catheter, JR 6.0, 6F
• 50885672102901: Angiographic Catheter, JL 6.0, 6F
• 50885672102895: Angiographic Catheter, JR 5.0, 6F
• 50885672102888: Angiographic Catheter, JL 5.0, 6F
• 50885672102017: Angiographic Catheter, JL 3.5, 6F
• 50885672102000: Angiographic Catheter, JR 3.5, 6F
• 50885672005585: Angiographic Catheter, Talon I, 6F
• 50885672005578: Angiographic Catheter, Talon I, 6F
• 50885672005561: Angiographic Catheter, Talon I, 6F
• 50885672005554: Angiographic Catheter, Talon I, 5F
• 50885672005547: Angiographic Catheter, Talon I, 5F
• 50885672005530: Angiographic Catheter, Talon I, 5F
• 50885672004526: Angiographic Catheter, JL 4.5, 5F
• 50885672004519: Angiographic Catheter, JR 4.5, 5F
• 50885672003611: Angiographic Catheter, Internal Mammary, 5F
• 50885672002935: Angiographic Catheter, JL 5.0, 5F