LEEP Lateral Vaginal Retractor

GUDID 00888937016215

LEEP Lateral Vaginal Retractor - Coated

Coopersurgical, Inc.

Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable
Primary Device ID00888937016215
NIH Device Record Keyd5ee221c-f0f6-4ad4-ac98-9e6709e10bc6
Commercial Distribution StatusIn Commercial Distribution
Brand NameLEEP Lateral Vaginal Retractor
Version Model NumberF400
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter
Width23 Millimeter
Length157 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100888937016215 [Primary]

FDA Product Code

HDLRetractor, Vaginal

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


[00888937016215]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-24
Device Publish Date2022-11-16

Devices Manufactured by Coopersurgical, Inc.

60888937027176 - ERPeak2024-04-18 IVD Sample kit
60888937027183 - ERPeak2024-04-18 IVD Sample kit
60888937027190 - ERPeak2024-04-18 IVD Sample kit
60888937027206 - ERPeak2024-04-18 IVD Sample kit
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

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