Cer-View Lateral Wall Retractor (Medium)

GUDID 00888937018035

Cer-View Lateral Wall Retractor (Medium)

Coopersurgical, Inc.

Vaginal speculum, reusable
Primary Device ID00888937018035
NIH Device Record Keya0f8bbb9-f650-43d2-8412-5d0efa23d90a
Commercial Distribution StatusIn Commercial Distribution
Brand NameCer-View Lateral Wall Retractor (Medium)
Version Model Number64-310
Company DUNS801895244
Company NameCoopersurgical, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter
Width22 Millimeter
Length150 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100888937018035 [Primary]

FDA Product Code

HDLRetractor, Vaginal

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


[00888937018035]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-12-14
Device Publish Date2022-12-06

Devices Manufactured by Coopersurgical, Inc.

00888937028126 - Biopsy Medium2026-02-12 Biopsy Medium. 10 ml
00888937028157 - Sperm Freezing Medium2026-02-12 Sperm Freezing Medium. 10ml
00888937028218 - PVP Medium2026-02-12 PVP Medium with phenol red. 1 ml
60888937028272 - Universal IVF Medium2026-02-12 Universal IVF Medium. 60 ml
00888937028287 - Universal IVF Medium2026-02-12 Universal IVF Medium with phenol red. 60 ml
00888937028317 - UTM2026-02-12 UTM Transfer Medium with phenol red. 10 ml
00888937028324 - UTM2026-02-12 UTM Transfer Medium
00888937028577 - Flushing Medium2026-02-12 Flushing Medium without Heparin. 125 ml

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.