AccessGUDID - DEVICE: MENTOR SILTEX CONTOUR PROFILE Moderate (00081317001867)

GUDID

Device Identifier (DI) Information

Brand Name: MENTOR SILTEX CONTOUR PROFILE Moderate
Version or Model: 3542912
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 354-2912
Company Name: MENTOR TEXAS L.P.

Primary DI Number: 00081317001867
Issuing Agency: GS1
Commercial Distribution End Date: February 10, 2021
Device Count: 1
Labeler D-U-N-S® Number*: 167450993 *Terms of Use

Device Description: Saline Breast Implant with Diaphragm Valve, 275cc

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:	Yes
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?
64084	Saline-filled breast implant, unstructured, textured-surface	An implantable device designed to reconstruct or augment the breast that is composed of a silicone rubber outer shell, made of polysiloxane(s), with a single lumen inflated with sterile isotonic saline to the desired size; the shell surface is textured. The implant may be of fixed or adjustable volume and may be prefilled, partially filled, or empty and filled during the implantation procedure; the volume of saline solution in adjustable volume implants may be adjusted after implantation. The device may vary in shape, profile, volume and shell thickness.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
FWM	Prosthesis, breast, inflatable, internal, saline

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
P990075	000

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: 76796de6-6864-4a8c-8585-efcc09b2d72e
Public Version Date: February 11, 2021
Public Version Number: 5
DI Record Publish Date: September 17, 2014