Home GUDID 30841156100098 OPTISPHERE
Primary DI 30841156100098
Brand OPTISPHERE
Company TELEFLEX INCORPORATED
Model IPN913232
Catalog number OSL271
Device description OptiSphere, 5-pack, 700-1000 micron, 2mL fill
Published 2018-03-27
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name KRD Device, Vascular, for Promoting Embolization
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KRD Device, Vascular, For Promoting Embolization Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 30841156100098 Package GS1 5 In Commercial Distribution 10841156100094 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 30841156100098 30841156100098 10841156100094 10841156100094
GMDN Terms# Term, Definition table Term Definition Non-neurovascular embolization plug, animal-derived A sterile, bioabsorbable, preformed device made from animal-derived (e.g., porcine) materials intended to be implanted in a non-neurovascular blood vessel, permanently or long-term, to occlude blood flow typically for treatment of an aneurysm, tumour (e.g., nephroma, hepatoma, uterine fibroids), and/or arteriovenous malformation (AVM). It is typically in the form of a gelatin foam pledget and may be supplied with dedicated instruments for implantation. This device is not intended to be used in intracranial arteries or for other neurovascular applications.
Regulatory Flags# DUNS number 002348191 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit true Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00763000936594 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936600 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936617 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936624 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936631 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936648 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936655 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936662 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936679 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936686 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936693 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936709 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936716 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936723 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936730 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936747 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936754 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936761 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936778 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936785 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936792 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936808 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936815 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936822 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936839 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936846 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936853 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936860 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936877 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27 00763000936884 Concerto Versa™ MEDTRONIC, INC. KRD 2026-02-27