OES Choledochofiberscope
CHF-CB30L Translaparoscopic CH Oledochos
8manufacturers in China registered for this device type
2catalogue numbers in this listing
6510(k) clearances naming this product code
Who Else Makes It
Concentrated in Guangdong (3), Shanghai (3), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Ningbo Wise Optomech Technology Corporation | Ningbo | Zhejiang | Contract manufacturer | 4 |
| Micro-Tech (Nanjing) Co., Ltd. | Nan Jing | Jiangsu | Contract manufacturer | 49 |
| Shenzhen Hugemed Medical Technical Development Co., Ltd. | Shenzhen | Guangdong | Manufacturer | 22 |
| Zhuhai Pusen Medical Technology Co., Ltd. | Zhuhai | Guangdong | Manufacturer | 7 |
| Shanghai Seegen Photoelectric Technology Co., Ltd. | Shanghai | Shanghai | Manufacturer | 7 |
| Eternal (Shanghai) Medical Technology Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 7 |
| Shenzhen Besdata Technology Co., Ltd. | Shenzhen | Guangdong | Manufacturer | 6 |
| Shanghai AnQing Medical Instrument Co., Ltd. | Shanghai | Shanghai | Manufacturer | 5 |
Record
| Listed by | Olympus Medical Systems Corp., Japan |
|---|---|
| FDA product code | FBN |
| Device type | Choledochoscope And Accessories, Flexible/Rigid |
| Device class | Class 2 |
| Regulation | 21 CFR 876.1500 |
| Establishment | Specification developer, Manufacturer, Exporter |
| Record published | 2016-09-21 |
| Record revised | 2024-01-12 (version 6) |
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 |
| Distribution end date | 2024-01-11 |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| OLYMPUS CHF TYPE CB30L | Withdrawn | |
| OLYMPUS CHF TYPE CB30L | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Single-use Video Scope | Micro-Tech (Nanjing) Co., Ltd. | 24 |
| Choledochoscope And Accessories, Flexible/Rigid | Richard Wolf Gmbh | 8 |
| Single-Use Choledochoscope | Shenzhen Hugemed Medical Technical Development Co., Ltd. | 6 |
| Pentax | Hoya Corporation | 5 |
| Flexible Video-Choledo-Cysto-Ureteroscope | Shanghai SeeGen Photoelectric Technology Co., Ltd. (YinDu Road Factory) | 5 |
| Riwo | Richard Wolf Gmbh | 4 |
| Flexible Video-Choledochoscope | Shanghai SeeGen Photoelectric Technology Co., Ltd. (YinDu Road Factory) | 4 |
| WiScope® | OTU Medical Inc | 4 |
| Choledochoscope And Accessories, Flexible/Rigid | Karl Storz GmbH & Co. KG | 4 |
| OES Uretero-Reno Fiberscope | Olympus Medical Systems Corp. | 3 |
| Gyrus Acmi | Gyrus Acmi, Inc. | 3 |
| Fiber Pancreatoscope | Pentax of America, Inc. | 2 |
Showing 12 of 34. All products under Choledochoscope And Accessories, Flexible/Rigid
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K113120 | 2012-09-25 |
| K093507 | 2010-03-10 |
| K081456 | 2008-11-06 |
| K082576 | 2008-10-21 |
| K080586 | 2008-05-06 |
| K051886 | 2005-11-14 |
Recalls Naming This Product
1 recall names this product by its own identifier, the UDI on its label.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Aizu Olympus Co., Ltd. | UDI-DI | 2023-09-25 | Class III | 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 | 3 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.