VYGON

Primary DI
00849884007435
Brand
VYGON
Company
Vygon Corporation
Model
2015SPI
Catalog number
2015SPI
Device description
POLYSITE ®Pressure injectable Implantable Infusion Port with silicone-filled suture holes
Published
2026-05-22
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

Related Records

Product Codes

CodeName
LJTPORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR

Product Code Classifications

CodeDeviceSpecialtyClass
LJTPort & Catheter, Implanted, Subcutaneous, IntravascularGeneral Hospital2

Premarket Submissions

SubmissionSupplement
K122834000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K122834000POLYSITE IMPLANTABLE INFUSION PORTSPerouse Medical2013-12-11LJT

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
20849884007439PackageGS11In Commercial Distribution
30849884007436PackageGS130In Commercial Distribution
00849884007435PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
2084988400743920849884007439
3084988400743630849884007436
00849884007435008498840074358498840074350849884007435

GMDN Terms

TermDefinition
Vascular port/catheterA fully-implantable device assembly intended to provide access to arteries/veins (excludes coronary and intracerebral circulation) for infusion (e.g., chemotherapeutic agents, blood transfusions) and/or drainage (e.g., blood). It consists of: 1) a subcutaneous chamber, with a self-sealing puncturable septum for percutaneous insertion of a hypodermic needle; and 2) an attached catheter which passes into the arteries/veins. It may consist of two chambers attached to a dual-lumen catheter for simultaneous infusion. It is made of metal [e.g., titanium (Ti)] and/or synthetic polymers (e.g., silicone); disposable devices associated with implantation may be included.

Regulatory Flags

DUNS number
120818216
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

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30849884007214VYGONAMS-9777CPAMS-9777CP2025-09-26
30849884007047VYGONVYML4D1003-1 VYML4D1003-1 2025-09-25
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