Single Use 3-Lumen Extraction Balloon V

GUDID 14953170368704

OLYMPUS MEDICAL SYSTEMS CORP.

Biliary stone retrieval balloon catheter

• Primary Device ID: 14953170368704
• NIH Device Record Key: 6105a1b2-bf6f-480f-bb7e-990c3acf3d41
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Single Use 3-Lumen Extraction Balloon V
• Version Model Number: B-V233P-A
• Company DUNS: 711789789
• Company Name: OLYMPUS MEDICAL SYSTEMS CORP.
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170368707 [Primary]
GS1	14953170368704 [Package]; Contains: 04953170368707; Package: [1 Units]; In Commercial Distribution
GS1	54953170368702 [Package]; Package: [15 Units]; In Commercial Distribution

FDA Product Code

• FGE: CATHETER, BILIARY, 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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-21

On-Brand Devices [Single Use 3-Lumen Extraction Balloon V]

• 14953170368773: B-V443Q-B
• 14953170368766: B-V443Q-A
• 14953170368759: B-V433P-B
• 14953170368742: B-V433P-A
• 14953170368735: B-V243Q-B
• 14953170368728: B-V243Q-A
• 14953170368711: B-V233P-B
• 14953170368704: B-V233P-A
• 14953170279567: Single Use 3-Lumen Extraction Balloon V
• 14953170279550: Single Use 3-Lumen Extraction Balloon V
• 14953170279529: Single Use 3-Lumen Extraction Balloon V
• 14953170279512: Single Use 3-Lumen Extraction Balloon V
• 14953170275767: Single Use 3-Lumen Extraction Balloon V
• 14953170275743: Single Use 3-Lumen Extraction Balloon V
• 14953170275705: Single Use 3-Lumen Extraction Balloon V
• 14953170275699: Single Use 3-Lumen Extraction Balloon V
• 14953170183451: Single Use 3-Lumen Extraction Balloon V
• 14953170183437: Single Use 3-Lumen Extraction Balloon V