Evis Exera III Colonovideoscope

2 catalogue numbers from OLYMPUS PCF-H190TI, listed by Olympus Medical Systems Corp., Japan, under Endoscope, Accessories, Narrow Band Spectrum. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

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

Chinese manufacturers registered for FDA product code NWB
Manufacturer City Province Registered as Device types
Qingdao O-MEC Medical Technology Co., Ltd. Qingdao Shandong Contract manufacturer 6
Scivita Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 19
Sonoscape Medical Corp. Shenzhen Guangdong Manufacturer 7

Record

Regulatory record for Evis Exera III Colonovideoscope
Listed by Olympus Medical Systems Corp., Japan
FDA product code NWB
Device type Endoscope, Accessories, Narrow Band Spectrum
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Specification developer, Manufacturer, Exporter
510(k) K192793
Record published 2020-08-27
Record revised 2024-04-22 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide, High-level Disinfectant
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Evis Exera III Colonovideoscope
Catalogue number Size Status
OLYMPUS PCF-H190TI In distribution
OLYMPUS PCF-HQ190L In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SonoScape Sonoscape Medical Corp. 10
Medisono Medisono, LLC 10
Evis Exera II Colonovideoscope Olympus Medical Systems Corp. 8
Rhino-Laryngo Videoscope Olympus Medical Systems Corp. 7
Evis Exera II Gastrointestinal Videoscope Olympus Medical Systems Corp. 7
Visera Cysto-Nephro Videoscope Olympus Medical Systems Corp. 6
Uretero-Reno Videoscope Olympus Medical Systems Corp. 4
Cysto-Nephro Videoscope Olympus Medical Systems Corp. 4
Olympus Olympus Winter & IBE Gmbh 4
Foot Holder Olympus Medical Systems Corp. 3
Light source cable Olympus Medical Systems Corp. 3
Foot Switch Olympus Medical Systems Corp. 3

Showing 12 of 66. All products under Endoscope, Accessories, Narrow Band Spectrum

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K100584 2010-07-02
K072957 2008-03-18
K062049 2006-09-22
K051645 2005-10-13

Recalls Naming This Product

3 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Evis Exera III Colonovideoscope
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Olympus Corporation of the Americas 510(k) number 2024-01-11 Class II Nonconforming Material/Component Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock loads. 1
Olympus Corporation of the Americas 510(k) number 2024-01-11 Class II Nonconforming Material/Component Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock loads. 28
Aizu Olympus Co., Ltd. 510(k) number 2023-09-25 Class II Under Investigation by firm Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead t 3101 units

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