Plug T4 PT4R-R
by Herniamesh
Plug T4 PT4R-R is a Class II device made by Herniamesh, listed in FDA GUDID since 8 Jan 2018 (UDI-DI 58032919891162), not in commercial distribution (GUDID) as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number58032919891162 | Date8 Jan 2018 | StatusListed |
Official records
- AccessGUDID record 58032919891162
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Plug T4
- Generic name
- Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable
- Model / reference
- PT4R-R
- Primary DI / UDI-DI
- 58032919891162
- FDA product code
- FTL
- GMDN term
- Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 878.3300
- GUDID distribution status
- Not in Commercial Distribution
Similar devices
Other devices filed under FDA product code FTL (Mesh, Surgical, Polymeric).
- Ltm-T Surgical Mesh by LIFECELL CORP
- Optilene Mesh by AESCULAP, INC.
- Optilene Mesh Lp by AESCULAP, INC.
- ATRIUM MEDICAL CORPORATION C-QUR MESH by Atrium Medical Corp.
- SOFT TISSUE AUGMENTATION TUBE (S.T.A.T.) by Tissue Technologies, Inc.
- Prolene Polypropylene Mesh Hernia Device by Ethicon Inc.
- Marlex Mesh Dart by C. R. Bard, Inc.
- Proceed Trilaminate Surgical Mesh by Ethicon Inc.
- 3DMAX Light Mesh, Models 0117310, 0117311, 0117312, 0117320, 0117321, 011732 by C. R. Bard, Inc.
- ENDOFAST RELIANT SYSTEM by Endogun Medical Systems