Primary Device ID | 00813570020787 |
NIH Device Record Key | 88c348b9-7365-4f1f-8567-fb124af87292 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Chord-X Premeasured Loops and Suture System |
Version Model Number | CXL-30-1838-20 |
Catalog Number | CXL-30-1838-20 |
Company DUNS | 844782318 |
Company Name | ON-X LIFE TECHNOLOGIES, INC. |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com | |
Phone | 512-339-8000 |
onx@onxlti.com |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Outer Diameter | 0.2245 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813570020381 [Primary] |
GS1 | 00813570020787 [Package] Contains: 00813570020381 Package: [5 Units] In Commercial Distribution |
PAW | Nonabsorbable Expanded Polytetrafluoroethylene Surgical Suture For Chordae Tendinae Repair Or Replacement |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-06-25 |
Device Publish Date | 2015-12-01 |
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