Inrad

Primary DI
10817295020609
Brand
Inrad
Company
Inrad
Model
50019
Device description
Modified Cournand Needle, 19 ga, 2 1/8"
Published
2016-12-01
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DYBIntroducer, Catheter

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DYBIntroducer, CatheterCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K812973000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K812973000PERCUTANEOUS INTRODUCER COURNAND STYLEDip, Inc.1981-11-16DYB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10817295020609PackageGS120In Commercial Distribution
00817295020602PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1081729502060910817295020609
00817295020602008172950206028172950206020817295020602

GMDN Terms#

Term, Definition table
TermDefinition
Non-vascular catheter introduction setA collection of sterile, invasive devices intended to enable percutaneous Seldinger-type introduction of a non-vascular catheter (e.g., drainage catheter) into a body cavity or lumen (e.g., biliary tract, ureter); it is not intended for introduction of a peritoneal dialysis catheter. It includes multiple invasive access devices which typically include an introducer needle, introducer sheath with an inner dilator, and guidewire; the catheter is not included. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
6163017800sales@inradinc.com

Regulatory Flags#

DUNS number
940023385
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
00817295020442Inrad510182016-12-01
00817295020459Inrad510192016-12-01
00817295020466Inrad521182016-12-01
00817295020473Inrad520182016-12-01
00817295020480Inrad524192016-12-01
00817295020497Inrad522192016-12-01
00817295020503Inrad521192016-12-01
00817295020510Inrad550182016-12-01
00817295020527Inrad570182016-12-01
00817295020534Inrad550192016-12-01
00817295020541Inrad570192016-12-01
00817295020596Inrad500182016-12-01
00817295020602Inrad500192016-12-01
00817295020619Inrad9910142016-12-01
00817295020626Inrad9910162016-12-01
00817295020633Inrad9910182016-12-01
00817295020640Inrad9910202016-12-01
00817295020657Inrad9915162016-12-01
00817295020664Inrad9915142016-12-01
00817295020671Inrad9915182016-12-01

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Primary DI, Brand, Company table
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10884450114855Prelude IDeal™Merit Medical Systems, Inc.DYB2026-06-08
00850084947001Genie MAXCULTIV8 1, LLCDYB2026-05-29
G440VIZ1750MultiflexVizaramed, Inc.DYB2026-04-09
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