Primary Device ID | 00850025525077 |
NIH Device Record Key | aabf4b4d-822c-4e40-99dc-51f04ef58645 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SPEX35 |
Version Model Number | SPN35090US |
Company DUNS | 962545294 |
Company Name | REFLOW 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 |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Guidewire Diameter | 0.035 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850025525077 [Primary] |
GS1 | 10850025525074 [Package] Package: [5 Units] In Commercial Distribution |
DQY | Catheter, Percutaneous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-01 |
Device Publish Date | 2021-09-23 |
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00856492005111 | Spex Shapeable Support Catheter, 35X135cm |
00856492005104 | Spex Shapeable Support Catheter, 35X150cm |
00850025525091 | Spex Shapeable Support Catheter, 35 X 150cm, US |
00850025525084 | Spex Shapeable Support Catheter, 35 X 135cm, US |
00850025525077 | Spex Shapeable Support Catheter, 35 X 90cm, US |
00850025525060 | Spex Shapeable Support Catheter, 35 X 50cm, US |