Hermesh

Primary DI
58032919892244
Brand
Hermesh
Company
HERNIAMESH SRL
Model
H90611
Device description
Hermesh 9 cm 6x11 is a rectangular standard macroporous mesh in Polypropylene monofilament knitted with quadriaxial tecnology, indicated for the treatment of inguinal and ventral hernias with both open and laparoscopic techniques.
Published
2021-10-13
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
58032919892244PrimaryGS10
18032919892246Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
5803291989224458032919892244
1803291989224618032919892246

GMDN Terms#

Term, Definition table
TermDefinition
Abdominal hernia surgical mesh, synthetic polymer, non-bioabsorbable, non-antimicrobialA 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 does not include an antimicrobial agent(s), 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

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Primary DI, Brand, Company table
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