Cannula- Curette

GUDID 20888937000768

Flexible 7mm OD

Coopersurgical, Inc.

Endometrial biopsy kit
Primary Device ID20888937000768
NIH Device Record Key17e79763-41bc-4e2e-899c-efbf2f070e38
Commercial Distribution StatusIn Commercial Distribution
Brand NameCannula- Curette
Version Model NumberMX517
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter
Outer Diameter7 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100888937000764 [Primary]
GS120888937000768 [Package]
Contains: 00888937000764
Package: [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HHKCurette, Suction, Endometrial (And Accessories)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-15

Devices Manufactured by Coopersurgical, Inc.

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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

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