AccessGUDID - DEVICE: PLUG T4 (58032919891162)

GUDID

Device Identifier (DI) Information

Brand Name: PLUG T4
Version or Model: PT4R-R
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: HERNIAMESH SRL

Primary DI Number: 58032919891162
Issuing Agency: GS1
Commercial Distribution End Date: March 11, 2019
Device Count: 5
Labeler D-U-N-S® Number*: 459310140 *Terms of Use

Device Description: Plug T4 is a rigid pre-shaped mesh with eccentric hole knitted with Polypropylene monofilament, indicated in medium-large in direct inguinal hernias, to reduce the size of an enlarged internal ring and also reinforces the surrounding tissues.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
60300	Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable	An implantable material (e.g., flat sheet) made from a non-bioabsorbable synthetic polymer(s) [e.g., polyglycolic acid (PGA), polycarbonate (PC), polyglycolide or carbon fibres] intended for extra-gynaecological, non-dental tissue repair/reinforcement application(s) [e.g., pericardial reinforcement, plastic surgery, abdominal hernia repair]. Disposable devices associated with implantation may be supplied with the mesh.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
FTL	Mesh, Surgical, Polymeric

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 83cf02fd-52d1-49fe-a518-b6f00332084b
Public Version Date: June 10, 2022
Public Version Number: 6
DI Record Publish Date: January 08, 2018