PENTAX Medical
- Primary DI
- 04961333246632
- Brand
- PENTAX Medical
- Company
- HOYA CORPORATION
- Model
- ED32-i10
- Device description
- PENTAX Medical Video Duodenoscope ED32-i10
- Published
- 2022-02-02
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes#
| Code | Name |
|---|---|
| FDT | duodenoscope and accessories, flexible/rigid |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FDT | Duodenoscope And Accessories, Flexible/Rigid | Gastroenterology, Urology | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04961333246168 | Direct Marking | GS1 | 0 | |
| 04961333246632 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04961333246168 | 04961333246168 | 4961333246168 |
| 04961333246632 | 04961333246632 | 4961333246632 |
GMDN Terms#
| Term | Definition |
|---|---|
| Flexible video gastroduodenoscope | An endoscope with a flexible inserted portion intended for the visual examination and treatment of the upper gastrointestinal (GI) tract [oesophagus, stomach, and duodenum (the first part of the small intestine), including the pancreas and the bile duct]. It is inserted into the body through the mouth during gastroduodenoscopy. 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. It can be end-viewing (looking forward) or side-viewing (looking to one side) and is used for the cannulation of the pancreas and bile duct. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| High-level Disinfectant |
| Liquid Chemical |
Regulatory Flags#
- DUNS number
- 691519705
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- false
- Serial number
- true
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 14961333079343 | PENTAX | OF-B173 | 2023-07-31 | |
| 14961333085535 | PENTAX | OE-A41 | 2023-07-31 | |
| 14961333232960 | PENTAX Medical | OE-A62 | 2023-07-31 | |
| 04961333084753 | PENTAX | OF-B80 | 2023-07-31 | |
| 04961333225569 | PENTAX Medical | EB19-J10U | 2020-07-17 | |
| 04961333239825 | VIVIDEO | CP-1000 | 2024-02-07 | |
| 04961333244744 | DEFINA | EPK-3000 | 2020-07-17 | |
| 04961333245888 | PENTAX Medical | EG34-i10 | 2020-07-17 | |
| 04961333246779 | PENTAX | EC-3890Li | 2025-04-04 | |
| 04961333246830 | PENTAX | EC38-i10L | 2025-04-04 | |
| 04961333246847 | PENTAX | EG-2990i | 2025-04-04 | |
| 04961333246939 | PENTAX | EG29-i10 | 2025-04-04 | |
| 04961333248056 | PENTAX Medical | VNL11-J10 | 2022-02-02 | |
| 04961333248063 | PENTAX Medical | VNL8-J10 | 2022-02-02 | |
| 04961333248070 | PENTAX Medical | VNL15-J10 | 2022-02-02 | |
| 04961333248148 | PENTAX | EC-3890Li | 2020-12-14 | |
| 04961333248179 | PENTAX | EG-2990i | 2020-12-14 | |
| 04961333248209 | PENTAX | EC38-i10L | 2020-12-14 | |
| 04961333248315 | PENTAX | EG29-i10 | 2020-12-14 | |
| 04961333248483 | PENTAX Medical | EG29-i10c | 2020-12-14 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 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 |
| 04961333255801 | INSPIRA | HOYA CORPORATION | FDT | 2025-06-20 |
| 04961333255825 | INSPIRA | HOYA CORPORATION | FDT | 2025-06-20 |
| 05707480157167 | Ambu® aScope™ Duodeno 2 | Ambu A/S | FDT | 2025-03-29 |
| 04961333356355 | PENTAX Medical | HOYA CORPORATION | FDT | 2024-09-03 |
| 04961333356331 | PENTAX Medical | HOYA CORPORATION | FDT | 2024-09-03 |
| 05707480157143 | Ambu® aScope™ Duodeno 2 | Ambu A/S | FDT | 2024-07-19 |
| 05707480157136 | Ambu® aScope™ Duodeno 2 | Ambu A/S | FDT | 2024-07-19 |
| 04961333254910 | INSPIRA | HOYA CORPORATION | FDT | 2023-12-01 |
| 04961333247974 | INSPIRA | HOYA CORPORATION | FDT | 2023-09-16 |
| 14961333232960 | PENTAX Medical | HOYA CORPORATION | FDT | 2023-07-31 |
| 14961333232991 | PENTAX Medical | HOYA CORPORATION | FDT | 2023-07-31 |
| 14961333246233 | PENTAX Medical | HOYA CORPORATION | FDT | 2023-07-31 |
| 04961333084456 | PENTAX | HOYA CORPORATION | FDT | 2023-07-31 |
| 04961333084470 | PENTAX | HOYA CORPORATION | FDT | 2023-07-31 |
| 04961333232963 | PENTAX Medical | HOYA CORPORATION | FDT | 2023-07-31 |
| 04961333232994 | PENTAX Medical | HOYA CORPORATION | FDT | 2023-07-31 |
| 04961333246236 | PENTAX Medical | HOYA CORPORATION | FDT | 2023-07-31 |
| 04953170438066 | Air/water valve | OLYMPUS MEDICAL SYSTEMS CORP. | FDT | 2023-04-22 |
| 04953170438349 | CONNECTING TUBE | OLYMPUS MEDICAL SYSTEMS CORP. | FDT | 2023-04-19 |
| 04953170441271 | SINGLE USE DISTAL COVER | OLYMPUS MEDICAL SYSTEMS CORP. | FDT | 2022-06-01 |
| 14953170441278 | SINGLE USE DISTAL COVER MAJ-2315 | OLYMPUS MEDICAL SYSTEMS CORP. | FDT | 2022-06-01 |
| 04953170452024 | EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V | OLYMPUS MEDICAL SYSTEMS CORP. | FDT | 2022-06-01 |
| 05707480157402 | aScope™ Duodeno | Ambu A/S | FDT | 2022-04-19 |
| 05707480157426 | aScope™ Duodeno | Ambu A/S | FDT | 2022-04-19 |
| 04961333246168 | N/A | HOYA CORPORATION | FDT | 2022-02-02 |
| 04953170063749 | EYEPIECE CAP | OLYMPUS MEDICAL SYSTEMS CORP. | FDT | 2021-12-20 |
| 04953170064012 | LIGHTGUIDE CAP | OLYMPUS MEDICAL SYSTEMS CORP. | FDT | 2021-12-20 |
| 03700712417512 | Maquet PowerLED II | MAQUET SAS | FDT | 2021-07-29 |