Pathfinder® Endoscope Cap GI EC-0412-1
GUDID 00850006222032
NEPTUNE MEDICAL INC.
Endoscope observation cap, single-use| Primary Device ID | 00850006222032 |
| NIH Device Record Key | cc2f9ee0-937e-44ae-b37f-d68741feb67b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pathfinder® Endoscope Cap |
| Version Model Number | GI EC-0412-1 |
| Catalog Number | GI EC-0412-1 |
| Company DUNS | 075588994 |
| Company Name | NEPTUNE MEDICAL INC. |
| 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 |
Customer Support Contacts
Device Dimensions
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
| Lumen/Inner Diameter | 12 Millimeter |
| Depth | 4 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850006222032 [Primary] |
FDA Product Code
| FDS | Gastroscope And Accessories, Flexible/Rigid |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-06-10 |
| Device Publish Date | 2021-06-02 |
Devices Manufactured by NEPTUNE MEDICAL INC.
| 00850006222322 - Pathfinder® CR System | 2024-07-17 The Pathfinder® CR System is a disposable endoscopy fluid management system for the 14mm ID Pathfinder®Endoscope Overtube. It |
| 00850006222025 - Pathfinder® Endoscope Overtube with Balloon | 2023-11-28 |
| 00850006222124 - Pathfinder® Endoscope Overtube with Balloon | 2023-11-28 |
| 00850006222049 - Pathfinder® Endoscope Overtube | 2021-09-08 |
| 00850006222056 - Pathfinder® Endoscope Overtube | 2021-09-08 |
| 00850006222063 - Pathfinder® Endoscope Overtube | 2021-09-08 |
| 00850006222070 - Pathfinder® Endoscope Overtube | 2021-06-15 |
| 00850006222087 - Pathfinder® Endoscope Overtube | 2021-06-15 |
Trademark Results [Pathfinder]
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