Prelude® PRO PRO-5F-11-035

GUDID 20884450707320

Merit Medical Systems, Inc.

Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable Vascular catheter introduction set, nonimplantable
Primary Device ID20884450707320
NIH Device Record Key3661f727-499d-4830-9724-290cebef5b7f
Commercial Distribution StatusIn Commercial Distribution
Brand NamePrelude® PRO
Version Model NumberF
Catalog NumberPRO-5F-11-035
Company DUNS184763290
Company NameMerit Medical Systems, Inc.
Device Count5
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100884450707326 [Unit of Use]
GS110884450707323 [Primary]
GS120884450707320 [Package]
Contains: 10884450707323
Package: [4 Units]
In Commercial Distribution

FDA Product Code

DREDILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-18
Device Publish Date2024-03-09

On-Brand Devices [Prelude® PRO]

2088445061437610884450614379
2088445061435210884450614355
2088445061434510884450614348
2088445061432110884450614324
2088445061431410884450614317
2088445061423910884450614232
2088445061422210884450614225
2088445061418510884450614188
2088445061412310884450614126
2088445061410910884450614102
2088445061404810884450614041
2088445061430710884450614300
2088445061403110884450614034
2088445061390410884450613907
2088445061395910884450613952
2088445061441310884450614416
2088445061421510884450614218
2088445061442010884450614423
2088445061436910884450614362
2088445061424610884450614249
2088445061397310884450613976
2088445061414710884450614140
2088445061393510884450613938
2088445061391110884450613914
2088445061396610884450613969
2088445061407910884450614072
2088445061420810884450614201
2088445061439010884450614393
2088445061392810884450613921
2088445061394210884450613945
2088445070843310884450708436
20884450708334F
20884450709553F
20884450709546F
20884450709508F
20884450707320F
20884450705319F
20884450709270F
20884450708501F
20884450709256F
20884450708372F
20884450709539F
20884450709225F
20884450708808F
20884450705166F
20884450709218F
20884450709515F
20884450709560F
20884450709232F
20884450709201F

Trademark Results [Prelude]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PRELUDE
PRELUDE
98418557 not registered Live/Pending
Blue Skies Collective LLC
2024-02-23
PRELUDE
PRELUDE
98132342 not registered Live/Pending
Honda Motor Co., Ltd.
2023-08-15
PRELUDE
PRELUDE
97808355 not registered Live/Pending
Everi Payments Inc.
2023-02-23
PRELUDE
PRELUDE
97808334 not registered Live/Pending
Everi Payments Inc.
2023-02-23
PRELUDE
PRELUDE
97711749 not registered Live/Pending
Honda Motor Co., Ltd.
2022-12-09
PRELUDE
PRELUDE
97700840 not registered Live/Pending
PRELUDE RESEARCH, INC.
2022-12-01
PRELUDE
PRELUDE
97698148 not registered Live/Pending
Thorlabs, Inc.
2022-11-30
PRELUDE
PRELUDE
97614908 not registered Live/Pending
Thorlabs, Inc.
2022-09-30
PRELUDE
PRELUDE
97593608 not registered Live/Pending
Darton Archery LLC
2022-09-15
PRELUDE
PRELUDE
97412434 not registered Live/Pending
PRELUDE RESEARCH, INC.
2022-05-16
PRELUDE
PRELUDE
97266044 not registered Live/Pending
Infinite Creative Enterprises, Inc.
2022-02-14
PRELUDE
PRELUDE
97033227 not registered Live/Pending
Prelude Products, Inc.
2021-09-17

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.