PENTAX Medical
- Primary DI
- 04961333356355
- Brand
- PENTAX Medical
- Company
- HOYA CORPORATION
- Model
- ED34-i10T2s
- Device description
- PENTAX Medical Video Duodenoscope ED34-i10T2s
- Published
- 2024-09-03
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Product Codes#
Product Code Classifications#
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K233942 | 000 |
Premarket Details#
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|---|---|---|---|---|
| K233942 | 000 | PENTAX Medical Video Duodenoscope (ED34-i10T2s); PENTAX Medical Video Processor (EPK-i8020c); PENTAX Medical Single Use, Sterile Distal End Cap with Elevator (OE-A63); Gas/Water Feeding Valves (OF-B194 ) | Pentax of America, Inc. | 2024-08-01 | FDT |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04961333356331 | Direct Marking | GS1 | 0 | |
| 04961333356355 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04961333356331 | 04961333356331 | 4961333356331 |
| 04961333356355 | 04961333356355 | 4961333356355 |
GMDN Terms#
| Term | Definition |
|---|---|
| Flexible video duodenoscope, reusable | An endoscope with a flexible inserted portion intended for the visual examination and treatment of the duodenum (the first part of the small intestine). It is inserted into the body through the mouth during duodenoscopy. Anatomical images are transmitted to the user by a video system with a charge-coupled device (CCD) chip at the distal end of the endoscope and the images showing on a monitor. This device is commonly used to examine structures and mucous membranes of the duodenum for conditions like ulcers, polyps, and cancer. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| "[""High-level Disinfectant"", ""Liquid Chemical"", ""Hydrogen Peroxide""]" |
Regulatory Flags#
- DUNS number
- 691519705
- Device count
- 1
- Serial number
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 04961333227747 | PENTAX | BS-LC1 | 2017-04-07 | |
| 04961333228362 | PENTAX | EG-3670URK | 2017-04-07 | |
| 04961333228409 | PENTAX | EG-3870UTK | 2017-04-07 | |
| 04961333233793 | PENTAX | EG-3270UK | 2018-08-10 | |
| 04961333254316 | PENTAX | EC-2990Li | 2024-07-26 | |
| 04961333254323 | PENTAX | EC34-i10L | 2024-07-26 | |
| 04961333254330 | PENTAX | EC-3890TLK | 2024-07-26 | |
| 04961333254347 | PENTAX | EC38-i10L | 2024-07-26 | |
| 04961333254354 | PENTAX | EC-3890Li | 2024-07-26 | |
| 04961333254385 | PENTAX | EG-2490K | 2024-07-26 | |
| 04961333254392 | PENTAX | EG27-i10 | 2024-07-26 | |
| 04961333254408 | PENTAX | EG-2990i | 2024-07-26 | |
| 04961333254422 | PENTAX | EG29-i10 | 2024-07-26 | |
| 04961333254439 | PENTAX | EG-3890TK | 2024-07-26 | |
| 04961333255238 | VIVIDEO | CP-1000 | 2025-12-19 | |
| 04961333255306 | VIVIDEO | VNL9-CP | 2025-12-19 | |
| 04961333255191 | VIVIDEO | CP-1000 | 2025-12-19 | |
| 04961333255245 | VIVIDEO | VNL9-CP | 2025-12-19 | |
| 04961333254620 | PENTAX Medical | OE-B17 | 2024-12-13 | |
| 04961333077731 | PENTAX | OF-B161 | 2023-07-31 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 04547410480269 | FUJIFILM | FUJIFILM CORPORATION | FET | 2026-05-22 |
| 00840432200063 | CystoView™ | Verathon Medical (Canada) ULC | FET | 2026-05-15 |
| 00840432200117 | CystoView™ | Verathon Medical (Canada) ULC | FET | 2026-05-15 |
| 00840432200308 | CystoView™ | Verathon Medical (Canada) ULC | FET | 2026-05-15 |
| 00840432200315 | CystoView™ | Verathon Medical (Canada) ULC | FET | 2026-05-15 |
| 00840432200322 | CystoView™ | Verathon Medical (Canada) ULC | FET | 2026-05-15 |
| 04953170467370 | SINGLE USE DISTAL COVER | OLYMPUS MEDICAL SYSTEMS CORP. | FDT | 2026-03-06 |
| 14953170467377 | SINGLE USE DISTAL COVER | OLYMPUS MEDICAL SYSTEMS CORP. | FDT | 2026-03-06 |
| 04049047788553 | Gimmi | Gimmi GmbH | FET | 2026-03-04 |
| 04049047788577 | Gimmi | Gimmi GmbH | FET | 2026-03-04 |
| 04049047788584 | Gimmi | Gimmi GmbH | FET | 2026-03-04 |
| 06971176282399 | Eview | Zhuhai Pusen Medical Technology Co, Ltd | FET | 2026-01-22 |
| 06972520300677 | Endoscopic Video Image Processor | Guangzhou Red Pine Medical Instrument Co., Ltd. | FET | 2025-12-31 |
| 05391533810088 | ProVee Video Processing Unit | PROVERUM LIMITED | FET | 2025-12-02 |
| 05391533810095 | ProVee Video Processing Unit | PROVERUM LIMITED | FET | 2025-12-02 |
| 04953170445538 | OTV-S700 UPGRADE PACK IR | OLYMPUS MEDICAL SYSTEMS CORP. | FET | 2025-11-21 |
| 04048551418123 | n.a. | Karl Storz GmbH & Co. KG | FET | 2025-08-11 |
| 04961333255801 | INSPIRA | HOYA CORPORATION | FDT | 2025-06-20 |
| 04961333255801 | INSPIRA | HOYA CORPORATION | FET | 2025-06-20 |
| 04961333255825 | INSPIRA | HOYA CORPORATION | FET | 2025-06-20 |
| 04961333255825 | INSPIRA | HOYA CORPORATION | FDT | 2025-06-20 |
| 04250480104200 | NA | SCHÖLLY FIBEROPTIC GmbH | FET | 2025-06-11 |
| 04250480104262 | N/A | SCHÖLLY FIBEROPTIC GmbH | FET | 2025-06-11 |
| 04547410513790 | FUJIFILM | FUJIFILM CORPORATION | FET | 2025-05-31 |
| 04953170430268 | 4K Camera Head | OLYMPUS MEDICAL SYSTEMS CORP. | FET | 2025-04-17 |
| 04953170433313 | VISERA ELITE III VIDEO SYSTEM CENTER | OLYMPUS MEDICAL SYSTEMS CORP. | FET | 2025-04-17 |
| 04953170433412 | VISERA ELITE III LED LIGHT SOURCE | OLYMPUS MEDICAL SYSTEMS CORP. | FET | 2025-04-17 |
| 04953170445453 | OTV-S700 UPGRADE PACK 3D | OLYMPUS MEDICAL SYSTEMS CORP. | FET | 2025-04-17 |
| 05707480157167 | Ambu® aScope™ Duodeno 2 | Ambu A/S | FDT | 2025-03-29 |
| 04048551432259 | NA | Karl Storz GmbH & Co. KG | FET | 2025-03-27 |