FDA UDI In Commercial Distribution 🇺🇸 United States

Hermesh

DI: 18032919892291 · Model: H95050 · HERNIAMESH SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hermesh
Primary DI
18032919892291
Version / Model
H95050
Company Name
HERNIAMESH SRL
Labeler DUNS
459310140
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-13
Public Version
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
beef860a-2721-4e82-b5bc-25ef62bead20

Device Description

Hermesh 9 cm 50x50 is a square 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.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FTL Mesh, Surgical, Polymeric

GMDN Terms

Code Name
60300 Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable

Identifiers

Type ID
Primary 18032919892291

Premarket Submissions

Submission Number Supplement Number
K973955 000