EndoVive Jejunal Feeding Tube

3-Port Through-the-PEG J-Tube Kit

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (1), Zhejiang (1), Shandong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code FPD
Manufacturer City Province Registered as Device types
ShanDong WeiGao Group Medical Polymer Co., Ltd. Weihai Shandong Contract manufacturer 3
VR Medical Technology Co., Ltd. Kunshan Jiangsu Contract manufacturer 13
Ningbo Tianyi Medical Appliance Co., Ltd. Ningbo Zhejiang Contract manufacturer 11

Record

Regulatory record for EndoVive Jejunal Feeding Tube
Listed by Boston Scientific Corporation, United States
FDA product code FPD
Device type Tube, Feeding
Device class Class 2
Regulation 21 CFR 876.5980
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-09-24
Record revised 2022-04-08 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for EndoVive Jejunal Feeding Tube
Catalogue number Size Status
M00566350 68 cm Effective Length In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Vygon Vygon Corp. 236
Ameritus Kentec Medical, LLC 83
Avanos Avanos Medical, Inc. 51
Halyard Avanos Medical, Inc. 50
Ameritus ENFit Kentec Medical, LLC 38
MED-RX Canadian Hospital Specialties Ltd. 28
DeRoyal Deroyal Industries, Inc. 20
ENFit SIL Feeding Tube Avanos Medical, Inc. 18
NeoConnect Enteral Feeding Tube Neomed Co., Ltd. 18
TubeClear Actuated Medical, Inc. 14
Corflo Ultra Lite NG Corpak Medsystems 13
Aquarius Degania Silicone, Ltd. 11

Showing 12 of 33. All products under Tube, Feeding

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K091340 2009-06-09
K971906 1997-08-20

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