Primary Device ID | 18032919891362 |
NIH Device Record Key | 7639068d-8f54-4529-b55e-acb74a50660a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HERTRA |
Version Model Number | HTR60513 |
Company DUNS | 459310140 |
Company Name | HERNIAMESH SRL |
Device Count | 5 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 18032919891362 [Unit of Use] |
GS1 | 58032919891360 [Primary] |
FTL | Mesh, Surgical, Polymeric |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-02 |
Device Publish Date | 2024-03-25 |
18032919892383 | Hertra 9 5.5x13 cm is a macroporous preshaped mesh with keyhole opening, indicated for the treat |
18032919891744 | Hertra 9A 4.5x10 cm is a macroporous preshaped mesh without keyhole opening, indicated for the t |
18032919891737 | Hertra 9 4.5x10 cm is a macroporous preshaped mesh with keyhole opening, indicated for the trea |
18032919891690 | Hertra 9A 5x11 cm is a macroporous preshaped mesh without keyhole opening, indicated for the tre |
18032919891683 | Hertra 9 5x11 cm is a macroporous preshaped mesh with keyhole opening, indicated for the treatme |
18032919891362 | Hertra 6 cm 5,5x13 is a light macroporous pre-shaped mesh, with hole, knitted with Polypropylene |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HERTRA 79047789 3547083 Live/Registered |
HERNIAMESH S.R.L. 2007-11-20 |