Seplou

The Ureteral Access Sheath is used to establish a conduit during endoscopic urological procedures facilitating the passage of endoscopes and other instruments into the urinary tract. It is…

Registry build 21.09.26

The Ureteral Access Sheath is used to establish a conduit during endoscopic urological procedures facilitating the passage of endoscopes and other instruments into the urinary tract. It is designed to establish a conduit for the treatment of urinary stones or other urinary diseases during the endoscopic procedures.

19manufacturers in China registered for this device type
24catalogue 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 Seplou
Listed by Seplou (Zhuhai) Co., Ltd., China
FDA product code FED
Device type Endoscopic Access Overtube, Gastroenterology-Urology
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Manufacturer
Record published 2025-09-17
Record revised 2026-07-09 (version 2)

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
Distribution end date 2026-05-07

Catalogue Numbers

Catalogue numbers for Seplou
Catalogue number Size Status
SPAS1245 In distribution
SPAS1345 In distribution
SPAS1045 In distribution
SPAS1145 In distribution
SPAS1445 In distribution
SPAS1250S In distribution
SPAS1140S In distribution
SPAS1135 In distribution
SPAS1435 In distribution
SPAS1050S In distribution
SPAS1335 In distribution
SPAS1340S In distribution
SPAS1028 In distribution
SPAS1040S In distribution
SPAS1033S In distribution
SPAS1350S In distribution
SPAS1145S In distribution
SPAS1245S In distribution
SPAS1240S In distribution
SPAS1035 In distribution
SPAS1345S In distribution
SPAS1235 In distribution
SPAS1150S In distribution
SPAS1045S Withdrawn

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
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
Forté® HD 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
K243025 2025-01-30

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