00712031

GUDID 10816765011949

Ponsky Guidewire Cholangiography System Round Tip

US Endoscopy

Cholangiopancreatography catheter, single-use

• Primary Device ID: 10816765011949
• NIH Device Record Key: 98b3385a-3be9-4588-9f6e-912abcefc949
• Commercial Distribution Discontinuation: 2019-03-25
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 00712031
• Catalog Number: 00712031
• Company DUNS: 627879687
• Company Name: US Endoscopy
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)769-8226
• Email: global@usendoscopy.com
• Phone: +1(800)769-8226
• Email: global@usendoscopy.com
• Phone: +1(800)769-8226
• Email: global@usendoscopy.com

Device Dimensions

• Length: 68 Centimeter
• Length: 68 Centimeter
• Length: 68 Centimeter

Operating and Storage Conditions

• Storage Environment Temperature: Between 15 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816765011942 [Primary]
GS1	10816765011949 [Package]; Contains: 00816765011942; Package: Box [5 Units]; Discontinued: 2019-03-25; Not in Commercial Distribution

FDA Product Code

• GCA: CATHETER, BILIARY, SURGICAL

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: 2019-04-05
• Device Publish Date: 2016-09-17

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