Wallace Ring Pessary PVC, 80 mm

GUDID 20888937020834

Wallace Ring Pessary PVC, 80 mm

Coopersurgical, Inc.

Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary Pelvic-organ-supporting pessary
Primary Device ID20888937020834
NIH Device Record Keyda3d86ca-17d3-4c9d-92a8-109621df3b8c
Commercial Distribution StatusIn Commercial Distribution
Brand NameWallace Ring Pessary PVC, 80 mm
Version Model Number700/300/080
Company DUNS801895244
Company NameCoopersurgical, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numbertrue
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter
Outer Diameter80 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100888937020830 [Primary]
GS120888937020834 [Package]
Contains: 00888937020830
Package: Box [20 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HHWPessary, Vaginal

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-01-28
Device Publish Date2020-01-20

Devices Manufactured by Coopersurgical, Inc.

00888937026870 - Mara Console2024-03-21 Mara Console- Endometrial Ablation
00888937023817 - K-Systems2024-02-27 L126 IVF, Standard Heat Right
00888937023824 - K-Systems2024-02-27 L126 IVF, Standard Heat Right
00888937023831 - K-Systems2024-02-27 L126 IVF, RI Witness Right
00888937023848 - K-Systems2024-02-27 L126 IVF, RI Witness Right
00888937023855 - K-Systems2024-02-27 L126 IVF, Standard Heat Right, Monitor
00888937023862 - K-Systems2024-02-27 L126 IVF, Standard Heat Right, Monitor
00888937023879 - K-Systems2024-02-27 L126 IVF, RI Witness Right, Monitor

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.