Fujifilm

This product is intended to be used in combination with an endoscope to assist endoscopic insertion into the body. Never use this product for any other purpose. This product is intended for…

Registry build 21.09.26

This product is intended to be used in combination with an endoscope to assist endoscopic insertion into the body. Never use this product for any other purpose. This product is intended for use in medical facilities by medical professionals who are properly trained in using it as well as in endoscopic procedures and endoscopic treatments.

19manufacturers in China registered for this device type
6catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (10), Shanghai (4), Zhejiang (3). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code FED
Manufacturer City Province Registered as Device types
Guangdong MacroLux Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 9
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Well Lead Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 46
Zhejiang Chuangxiang Medical Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Jiana Sterilization Technology (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 23
Shenzhen Hugemed Medical Technical Development Co., Ltd. Shenzhen Guangdong Manufacturer 22
Macrolux Medical Technology Co., Ltd. Shenzhen Guangdong Manufacturer 9
Zhuhai Pusen Medical Technology Co., Ltd. Zhuhai Guangdong Manufacturer 7
Seplou (Zhuhai) Co., Ltd. Zhuhai Guangdong Manufacturer 7
Zhejiang Yigao Medical Technology Co., Ltd. Hangzhou Zhejiang Manufacturer 7
Eternal (Shanghai) Medical Technology Co., Ltd. Shanghai Shanghai Contract manufacturer 7

Showing 12 of 19. All 19 manufacturers in China registered for Endoscopic Access Overtube, Gastroenterology-Urology

Record

Regulatory record for Fujifilm
Listed by Fujifilm Corporation, Japan
FDA product code FED
Device type Endoscopic Access Overtube, Gastroenterology-Urology
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K091773
Record published 2016-10-18
Record revised 2024-06-07 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date
Storage Handling environment atmospheric pressure 70 to 106 KiloPascal; Storage environment temperature 10 to 40 °C; Handling environment humidity 30 to 85 % RH; Storage environment humidity 30 to 85 % RH; Handling environment temperature 10 to 40 °C; Storage environment atmospheric pressure 70 to 106 KiloPascal
Packaging Box

Catalogue Numbers

Catalogue numbers for Fujifilm
Catalogue number Size Status
TS-12140 In distribution
TR-1504A In distribution
TR-1507A In distribution
TR-1108A In distribution
TS-13101 In distribution
TR-1208A In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ClearPetra Well Lead Medical Co., Ltd. 175
CoralWell Macrolux Medical Technology Co., Ltd. 56
Single Use Ureteral Access Sheath Zhejiang Chuangxiang Medical Technology Co., Ltd. 35
Single-use Ureteral Access Sheath Shenzhen Hugemed Medical Technical Development Co., Ltd. 25
Flexor Cook Incorporated 25
Seplou Seplou (Zhuhai) Co., Ltd. 24
Flexor Parallel Cook Incorporated 21
Single-use Ureteral Access Sheath Hunan Vathin Medical Instrument Co., Ltd. 20
Ureteral Access Sheath Well Lead Medical Co., Ltd. 18
Guardus Us Endoscopy 16
Porges Coloplast Coloplast A/S 14
Forté® AXP Access Sheath Applied Medical Resources Corp. 13

Showing 12 of 66. All products under Endoscopic Access Overtube, Gastroenterology-Urology

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243091 2024-11-01

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