Hermesh

Primary DI
18032919890532
Brand
Hermesh
Company
HERNIAMESH SRL
Model
H42020
Device description
Hermesh 4 cm 20x20 is a square macroporous mesh, of standard weight, knitted with Polypropylene monofilament, indicated for the treatment of inguinal and ventral hernias, in both open and laparoscopic techniques.
Published
2021-10-13
Public version status
New
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
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
58032919890530PrimaryGS10
18032919890532Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
5803291989053058032919890530
1803291989053218032919890532

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
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
true
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
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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