Evis-EUS Connecting Cable E

Catalogue number MAJ-1711, listed by Olympus Medical Systems Corp., Japan, under Endoscopic Ultrasound System, Gastroenterology-Urology. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code ODG
Manufacturer City Province Registered as Device types
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49

Record

Regulatory record for Evis-EUS Connecting Cable E
Listed by Olympus Medical Systems Corp., Japan
FDA product code ODG
Device type Endoscopic Ultrasound System, Gastroenterology-Urology
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Specification developer, Manufacturer, Exporter
Record published 2017-10-12
Record revised 2023-01-16 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date
Distribution end date 2022-08-09

Catalogue Numbers

Catalogue numbers for Evis-EUS Connecting Cable E
Catalogue number Size Status
MAJ-1711 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pentax Hoya Corporation 22
Areus(TM) Endoscopic Ultrasound Aspiration Needle (FNA) Micro-Tech (Nanjing) Co., Ltd. 12
Areus(TM) Adapt Endoscopic Ultrasound Aspiration Needle(FNA) Micro-Tech (Nanjing) Co., Ltd. 6
Pentax Medical Hoya Corporation 6
Water-resistant Cap Olympus Medical Systems Corp. 6
Expect Boston Scientific Corporation 4
Ultrasonic Probe Olympus Medical Systems Corp. 4
BALLOON3 Olympus Medical Systems Corp. 3
Acquire Boston Scientific Corporation 3
Evis-EUS Image Cable Olympus Medical Systems Corp. 3
Expect Slimline SL Boston Scientific Corporation 3
Evis Exera II Ultrasound Gastrovideoscope Olympus Medical Systems Corp. 2

Showing 12 of 52. All products under Endoscopic Ultrasound System, Gastroenterology-Urology

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K261183 2026-07-31
K251859 2025-10-03

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