FDA.reportPublic FDA data

OVAL PATCH

Primary DI
58032919890981
Brand
OVAL PATCH
Company
HERNIAMESH SRL
Model
OP1114
Device description
Oval patch cm 11x14 is an oval rigid mesh knitted with Polypropylene monofilament, it is indicated for use in open pre-peritoneal ventral hernia repairs, no suture are needed to secure the mesh
Published
2016-08-03
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
FTLMesh, Surgical, Polymeric

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FTLMesh, Surgical, PolymericGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K973955000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K973955000HERNIAMESH SURGICAL MESHESHerniamesh1998-05-11FTL

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
58032919890981PrimaryGS10
18032919890983Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
5803291989098158032919890981
1803291989098318032919890983

GMDN Terms#

Term, Definition table
TermDefinition
Abdominal hernia surgical mesh, synthetic polymer, non-bioabsorbableA sterile, flat or three-dimensional (3-D), woven/knitted or porous material made of one or more non-bioabsorbable synthetic polymers [e.g., polypropylene, polyethylene (PE)] intended to be permanently implanted for abdominal hernia (e.g., inguinal, ventral/incisional, umbilical, femoral) and fascial defect repair applications; it is not intended for extra-abdominal applications and not dedicated to diaphragmatic hernia repair. It is typically available with various material attributes and may be pre-configured or cut to a desired size/shape. Disposable devices associated with implantation (e.g., introducer needles, trocars) may be included.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
459310140
Device count
5
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
28032919891062PLUG T2PT2/32023-07-13
28032919891871PLUG T2PT2/3-H32023-07-14
58032919890530HermeshH420202021-10-13
58032919890752HermeshH610152021-10-13
58032919891049PLUG T1PT1/52023-07-13
58032919891056PLUG T1PT1/72023-07-13
58032919891179PLUG T4PT4R-S2023-07-13
58032919891254Round PatchH5C102021-10-13
58032919891360HERTRAHTR605132024-03-25
58032919891384HERTRA 5HTR505132021-10-13
58032919891681HERTRAHTR905112023-07-14
58032919891698HERTRAHTR9A5112023-07-14
58032919891735HERTRAHTR092023-07-14
58032919891742HERTRAHTR9A2023-07-14
58032919891797HERTRA 5HTR052021-10-13
58032919891827PLUG T4PT4R-Q2023-07-13
58032919892251HermeshH908152021-10-13
58032919892268HermeshH910152021-10-13
58032919892275HermeshH915152021-10-13
58032919892282HermeshH930302021-10-13

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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06970461300244TisuthesShanghai Suokang Medical Implants Co.,Ltd.FTL2026-07-22
06970461300251TisuthesShanghai Suokang Medical Implants Co.,Ltd.FTL2026-07-22
06970461300268TisuthesShanghai Suokang Medical Implants Co.,Ltd.FTL2026-07-22
06970461300275TisuthesShanghai Suokang Medical Implants Co.,Ltd.FTL2026-07-22
06970461300282TisuthesShanghai Suokang Medical Implants Co.,Ltd.FTL2026-07-22
06970461300299TisuthesShanghai Suokang Medical Implants Co.,Ltd.FTL2026-07-22
06970461300305TisuthesShanghai Suokang Medical Implants Co.,Ltd.FTL2026-07-22