SpyGlass
- Primary DI
- 08714729764441
- Brand
- SpyGlass
- Company
- BOSTON SCIENTIFIC CORPORATION
- Model
- M00546030
- Device description
- Direct Visualization Probe
- Published
- 2016-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
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 |
|---|---|---|---|---|
| 08714729764441 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 08714729764441 | 08714729764441 | 8714729764441 |
GMDN Terms#
| Term | Definition |
|---|---|
| ERCP catheter, non-balloon, non-electrical, reusable | A non-electrical flexible tube inserted through a flexible endoscope, after its placement in the duodenum via the oral cavity, for the endoscopic cannulation of the gastrointestinal ductal system (i.e., the pancreatic, hepatic, and/or common bile ducts) during endoscopic retrograde cholangiopancreatography (ERCP). It is typically a single-lumen device made of radiopaque plastic materials with incremental markings at the distal tip, used to deliver a contrast medium to the ducts for their radiographic visualization; it does not incorporate a balloon. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 |
Regulatory Flags#
- DUNS number
- 021717889
- Device count
- 1
- Lot or batch
- true
- Manufacturing date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 08714729424246 | Contour™ | M006180231120 | 2015-09-24 | |
| 08714729457923 | Percuflex™ | M006145360050 | 2015-09-24 | |
| 08714729460282 | Percuflex™ Plus | M006175198060 | 2015-09-24 | |
| 08714729460398 | Percuflex™ Plus | M006175250060 | 2015-09-24 | |
| 08714729460657 | Percuflex™ Plus | M006175260050 | 2015-09-24 | |
| 08714729461012 | Percuflex™ Plus | M006175265060 | 2015-09-24 | |
| 08714729766629 | Polaris™ Ultra | M006192140190 | 2015-09-24 | |
| 08714729766735 | Polaris™ Ultra | M006192144170 | 2015-09-24 | |
| 08714729766759 | Polaris™ Ultra | M006192145120 | 2015-09-24 | |
| 08714729766766 | Polaris™ Ultra | M006192145170 | 2015-09-24 | |
| 08714729766803 | Polaris™ Ultra | M006192150190 | 2015-09-24 | |
| 08714729766841 | Polaris™ Ultra | M006192152120 | 2015-09-24 | |
| 08714729766919 | Polaris™ Ultra | M006192154170 | 2015-09-24 | |
| 08714729766926 | Polaris™ Ultra | M006192154190 | 2015-09-24 | |
| 08714729776307 | Contour™ | M006180235170 | 2015-09-24 | |
| 08714729776680 | Contour™ | M006180230180 | 2015-09-24 | |
| 08714729777137 | Polaris™ Ultra | M006192140180 | 2015-09-24 | |
| 08714729777199 | Polaris™ Ultra | M006192150180 | 2015-09-24 | |
| 08714729777205 | Polaris™ Ultra | M006192151180 | 2015-09-24 | |
| 08714729777441 | Polaris™ Loop | M006155225090 | 2015-09-24 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 04580826921391 | PENTAX Medical | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 04580826921407 | PENTAX Medical | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 04580826921438 | PENTAX Medical | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 04580826926693 | PENTAX Medical | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 04580826926709 | PENTAX Medical | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 04580826926778 | PENTAX Medical | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 04580826926792 | PENTAX Medical | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 04580826928406 | PENTAX Medical | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 04580826928499 | PENTAX Medical | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 04580826930935 | INSPIRA | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 04580826930959 | INSPIRA | PENTAX MEDICAL CORPORATION | FDT | 2026-08-25 |
| 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 |