Primary Device ID | 00850006222025 |
NIH Device Record Key | 798f6471-105d-4fa7-b423-eca7180fb408 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pathfinder® Endoscope Overtube with Balloon |
Version Model Number | GI 110140B-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 |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com | |
Phone | 8882028401 |
info@neptunemedical.com |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Length | 110 Centimeter |
Catheter Working Length | 100 Centimeter |
Outer Diameter | 14 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850006222025 [Primary] |
FED | Endoscopic Access Overtube, Gastroenterology-Urology |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-11-28 |
Device Publish Date | 2023-11-20 |
00850006222124 | GI 085140B-1 |
00850006222025 | GI 110140B-1 |