Primary Device ID | 18032919891874 |
NIH Device Record Key | 892780f5-c87e-4193-a486-6f57eb24ef0d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PLUG T2 |
Version Model Number | PT2/3-H3 |
Company DUNS | 459310140 |
Company Name | HERNIAMESH SRL |
Device Count | 2 |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 18032919891874 [Unit of Use] |
GS1 | 28032919891871 [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 | 2023-07-24 |
Device Publish Date | 2023-07-14 |
18032919891874 | Plug T2 3 cm is a macroporous three-dimensional plug on a round base, indicated for treatment of |
18032919891898 | Plug T2 7 cm is a macroporous three-dimensional plug on a round base, indicated for treatment of |
18032919891881 | Plug T2 5 cm is a macroporous three-dimensional plug on a round base, indicated for treatment of |