Lubriglide

GUDID 08714729012610

Coated Guidewire

BOSTON SCIENTIFIC CORPORATION

Gastro-urological guidewire, single-use

Primary Device ID	08714729012610
NIH Device Record Key	e0aae34a-5275-45e5-ac78-b7cfeed239a5
Commercial Distribution Status	In Commercial Distribution
Brand Name	Lubriglide
Version Model Number	M0066001050
Company DUNS	021717889
Company Name	BOSTON SCIENTIFIC CORPORATION
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729012610 [Primary]

FDA Product Code

EZB	STYLET FOR CATHETER, GASTRO-UROLOGY

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	2024-12-23
Device Publish Date	2016-09-24

On-Brand Devices [Lubriglide]

08714729191131	Coated Guidewire
08714729057062	Coated Guidewire
08714729056645	Coated Guidewire
08714729012610	Coated Guidewire
08714729012603	Coated Guidewire
08714729012580	Coated Guidewire
08714729011392	Coated Guidewire
08714729011378	Coated Guidewire

Trademark Results [Lubriglide]

Mark Image Registration \| Serial	Company Trademark Application Date
LUBRIGLIDE 74485615 1949514 Live/Registered	SANFORD, L.P. 1994-02-02