Endogator Kit

Endagator Kit includes Endogator Irrigation Tubing, for Endogator EGP-100 Irrigation pump, Olympus OFP Pump, gi4000 ESU or Torrent Irrigation Pump. and ENDO SMARTCAP Rinse and Insufflation…

Registry build 21.09.26

Endagator Kit includes Endogator Irrigation Tubing, for Endogator EGP-100 Irrigation pump, Olympus OFP Pump, gi4000 ESU or Torrent Irrigation Pump. and ENDO SMARTCAP Rinse and Insufflation tubing for certain OLYMPUS GI Endoscopes.

10manufacturers in China registered for this device type
37catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (6), Zhejiang (3), Chongqing (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OCX
Manufacturer City Province Registered as Device types
Zhejiang Chuangxiang Medical Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Suzhou Jinsheng Plastic Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Forefront Medical Technology (Jiangsu) Co., Ltd. Changzhou Jiangsu Contract manufacturer 14
Smartdata Suzhou Co., Ltd. Suzhou Jiangsu Contract manufacturer 11
Yangzhou Fartley Medical Instrument Technology Co., Ltd. Yangzhou Jiangsu Contract manufacturer 24
Jiana Sterilization Technology (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 23
Hangzhou AGS MedTech Co., Ltd. Hangzhou Zhejiang Repacker / relabeller 19
Changzhou Intl. Trade & Enterprises Cooperative Co., Ltd. Changzhou Jiangsu Manufacturer 14
Changzhou Endoclean Medical Device Co., Ltd. Changzhou Jiangsu Repacker / relabeller 13
Chongqing Jinshan Science & Technology (Group) Co., Ltd. Chongqing Chongqing Manufacturer 4

Record

Regulatory record for Endogator Kit
Listed by Medivators Inc, United States
FDA product code OCX
Device type Endoscopic Irrigation/Suction System
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K102855
Record published 2018-08-16
Record revised 2023-01-04 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Packaging Case of 10, case of 30, carton of 10, case of 20, box of 10, box of 2
Distribution end date 2023-01-03

Catalogue Numbers

Catalogue numbers for Endogator Kit
Catalogue number Size Status
100652 In distribution
100623 In distribution
100653 In distribution
100618 In distribution
100650B In distribution
4005470 In distribution
4005472 In distribution
4005471 In distribution
100602 In distribution
100650 In distribution
100626 In distribution
100627 In distribution
100628 In distribution
100655B In distribution
100622B In distribution
100613 In distribution
100657 In distribution
100651 In distribution
100603 In distribution
100653B In distribution
100658 In distribution
100625 In distribution
100658B In distribution
100622 In distribution
100623B In distribution
100654 In distribution
100620B In distribution
100621 In distribution
100611 In distribution
100629 In distribution
100620 In distribution
100656 In distribution
100655 In distribution
100615 Withdrawn
100612 Withdrawn
100614 Withdrawn
100616 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Clean Connecting Tube Yangzhou Fartley Medical Instrument Technology Co., Ltd. 21
Erbe Erbe Elektromedizin GmbH 19
Endogator Medivators Inc 18
Torrent Us Endoscopy 14
ClearCap Distal Attachment Finemedix 14
EndoGator Hybrid Medivators Inc 13
Endoscopic Irrigation/Suction System Pentax of America, Inc. 12
Reveal Us Endoscopy 12
Endogator hybrid irrigation tubing Medivators Inc 10
Erbeflo® 2 Erbe Medical, LLC 9
BullDog® Diversatek Healthcare Inc 9
Olympus Keymed (Medical & Industrial Equipment) Ltd 8

Showing 12 of 123. All products under Endoscopic Irrigation/Suction System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K231418 2023-08-14
K140753 2014-07-15

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer