Prelude®

Primary DI
10884450415358
Brand
Prelude®
Company
Merit Medical Systems, Inc.
Model
J
Catalog number
PSI-4F-23MT
Published
2026-05-28
Public version status
New
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
CodeName
DREDILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DREDilator, Vessel, For Percutaneous CatheterizationCardiovascular2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20884450415355PackageGS14In Commercial Distribution
10884450415358PrimaryGS10
00884450415351Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2088445041535520884450415355
1088445041535810884450415358
00884450415351008844504153518844504153510884450415351

GMDN Terms#

Term, Definition table
TermDefinition
Vascular catheter introduction set, nonimplantableA collection of nonimplantable, invasive devices intended to provide percutaneous vascular access to enable introduction of a catheter (not included) into the vascular system. It includes a non-steerable introducer sheath with an inner obturator/dilator, and typically an additional access device(s) [e.g., guidewire, introducer needle, syringe, additional dilators] which may include a haemostatic valve to control blood loss, usually to enable arterial access. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Device Size Text, specify0

Regulatory Flags#

DUNS number
184763290
Device count
5
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#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00884450029695Merit Medical®Initial ReleaseK08-02207A2026-07-24
00884450383865Merit Medical®Initial ReleaseK10-01245L2026-07-25
00884450419922SureCrossDSC181352026-07-24
00884450428320Merit Medical®Initial ReleaseK09-10593C2026-07-24
00884450470831Merit Medical®Initial ReleaseK09-12157A2026-07-24
00884450484203Merit Medical®Initial ReleaseK09-144012026-07-24
00884450485569Merit Medical®Initial ReleaseK12T-127302026-07-24
00884450486214Merit Medical®Initial ReleaseK12T-12593A2026-07-24
00884450486955Merit Medical®Initial ReleaseK02-016512026-07-25
00884450545010Aspira®Initial Release49925242026-07-25
00884450545034Aspira®Initial Release4992524B2026-07-25
00884450793817BioFlo DuraMax®AH9651030380112026-07-25
00884450846148Merit Medical®Initial ReleaseK09-14237A2026-07-25
00884450433812Merit Medical®Initial ReleaseK08-02803A2026-07-23
00884450485163Merit Medical®Initial ReleaseK12T-11888B2026-07-23
00884450376546Merit Medical®Initial ReleaseK09-05229L2026-07-22
00884450431764Merit Medical®Initial ReleaseK10-04836A2026-07-22
00884450488751Merit Medical®Initial ReleaseK09-144102026-07-22
00884450492888Merit Medical®Initial ReleaseK01-08008A2026-07-22
00884450499276Merit Medical®Initial ReleaseK09-13679B2026-07-22

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
10884450708955Prelude®Merit Medical Systems, Inc.DRE2026-07-18
10884450415631Prelude®Merit Medical Systems, Inc.DRE2026-07-08
10884450415655Prelude®Merit Medical Systems, Inc.DRE2026-07-08
10884450707781Prelude®Merit Medical Systems, Inc.DRE2026-07-08
00884450860342Merit S-MAK™Merit Medical Systems, Inc.DRE2026-06-25
00884450468340Merit MAK™Merit Medical Systems, Inc.DRE2026-06-23
10884450706708Prelude®Merit Medical Systems, Inc.DRE2026-06-03
04251244502768Catapult Guide SheathContract Medical International GmbHDRE2024-08-19
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04251244501983Catapult Guide SheathContract Medical International GmbHDRE2023-09-01
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