17G Wallace Single Lumen Oocyte Needle

GUDID 30888937021142

17G Wallace Single Lumen Oocyte Needle (Box of 10)

Coopersurgical, Inc.

IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use IVF oocyte aspiration needle, single-use
Primary Device ID30888937021142
NIH Device Record Keye73979aa-92b9-4312-a85d-ab900dd18598
Commercial Distribution StatusIn Commercial Distribution
Brand Name17G Wallace Single Lumen Oocyte Needle
Version Model NumberON1733
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge
Needle Gauge17 Gauge

Device Identifiers

Device Issuing AgencyDevice ID
GS100888937021141 [Primary]
GS120888937021145 [Package]
Contains: 00888937021141
Package: Box [10 Units]
In Commercial Distribution
GS130888937021142 [Package]
Contains: 20888937021145
Package: Case [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQENeedle, Assisted Reproduction

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-12-12
Device Publish Date2019-12-04

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.