| Primary Device ID | 08714729764434 |
| NIH Device Record Key | 4921f999-1cf1-4bfe-b732-5bd1452b544e |
| Commercial Distribution Discontinuation | 2020-01-03 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | SpyScope |
| Version Model Number | M00546230 |
| Company DUNS | 021717889 |
| Company Name | BOSTON SCIENTIFIC CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08714729764434 [Primary] |
| ODF | Mini endoscope, gastroenterology-urology |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-10-20 |
| Device Publish Date | 2016-09-24 |
| 00191506060091 - OverStitch™ | 2025-09-29 Intragastric Balloon System |
| 08714729878018 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878025 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878049 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878056 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878063 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878070 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878087 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SPYSCOPE 78478444 3345106 Live/Registered |
BOSTON SCIENTIFIC SCIMED, INC. 2004-09-03 |
![]() SPYSCOPE 77555950 not registered Dead/Abandoned |
Novadaq Technologies Inc. 2008-08-26 |
![]() SPYSCOPE 74066242 not registered Dead/Abandoned |
Homespun Imports, Inc. 1990-06-06 |