Contour VL™

GUDID 08714729423812

Polymeric ureteral stent

Primary Device ID	08714729423812
NIH Device Record Key	ba8a3214-9cde-439d-b84b-7d729871bb4e
Commercial Distribution Discontinuation	2024-01-12
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	Contour VL™
Version Model Number	M006180156080
Company DUNS	021717889
Company Name	BOSTON SCIENTIFIC CORPORATION
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	false
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

Device Issuing Agency	Device ID
GS1	08714729423812 [Primary]

FAD	STENT, URETERAL

Steralize Prior To Use	false
Device Is Sterile	true

08714729423737	Variable Length Ureteral Stent Set
08714729423867	Variable Length Ureteral Stent Set
08714729423812	Variable Length Ureteral Stent Set
08714729423782	Variable Length Ureteral Stent Set
08714729423720	Variable Length Ureteral Stent Set
08714729068020	Variable Length Ureteral Stent
08714729067986	Variable Length Ureteral Stent
08714729058410	Variable Length Ureteral Stent