FDA.reportPublic FDA data

Procedure Products Needle

Primary DI
B1603118222
Brand
Procedure Products Needle
Company
PROCEDURE PRODUCTS, INC.
Model
31-1822
Device description
NEEDLE, W/O BASEPLATE 5.7CM 18g
Published
2017-02-07
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
CodeName
DREDilator, Vessel, For Percutaneous Catheterization

Product Code Classifications#

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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K810859000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K810859000SINGLE USE SELDINGER/COURNAND PERC. NDLProcedure Products, Inc.1981-04-11DRE

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B1603118222PackageHIBCC25In Commercial Distribution
B1603118221PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Vascular catheter introduction needleA sterile, sharp bevel-edged, hollow tubular metal instrument designed to make the initial percutaneous puncture to access a vein and/or artery during vascular catheterization. It is available in a variety of forms to enable a catheter to be introduced directly, or a guidewire to be introduced (Seldinger technique); the therapeutic or diagnostic aspiration of fluids may be achieved during its placement. Its lumen is not intended to be filled with an obturator/dilator and it does not include additional access devices. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
151507563
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
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
B1602118351Procedure Products Needles21-18352017-02-07
B1602293571Procedure Products needles229-3572017-04-03
B1603118221Procedure Products Needle31-18222017-02-07
B1603293551Procedure Products needles329-3552017-04-03
B1603293571Procedure Products Needle329-3572016-12-01
B1603118451Procedure Products Needle31-18452020-03-10
B1602018221Procedure Products needles20-18222017-04-03
B1602018271Procedure Products Needle20-18272016-12-01
B1602018401Procedure Products Needles20-184020-18402018-01-02
B1602118271Procedure Products Needle21-18272016-12-01
B160211827P1Procedure Products Needles21-1827-P2017-09-27
B1603118151Procedure Products Needles31-18152017-02-07
B1603118271Procedure Products Needle31-18272016-12-01
B160311827P1Procedure Products Needles31-1827-P2017-09-27
B1603118351Procedure Products Syringes31-18352017-02-07
B1603118601Procedure Products Needle31-186031-18602018-01-02
B1603121151Procedure Products Needle31-21152017-09-12
B16032M18601Procedure Products Needle32M-18602017-02-07
B1605118271Procedure Products Needle51-18272016-12-01
B1605518291Procedure Products Needles55-182955-18292018-01-02

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Primary DI, Brand, Company table
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00884450468340Merit MAK™Merit Medical Systems, Inc.DRE2026-06-23
10884450706708Prelude®Merit Medical Systems, Inc.DRE2026-06-03
10884450415358Prelude®Merit Medical Systems, Inc.DRE2026-05-28
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