Primary Device ID | 50849884005474 |
NIH Device Record Key | f560046e-6a33-440a-bc8b-0080dc4ccf9f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VYGON |
Version Model Number | VYLFM1003 |
Catalog Number | VYLFM1003 |
Company DUNS | 120818216 |
Company Name | Vygon 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00849884005479 [Primary] |
GS1 | 30849884005470 [Package] Contains: 00849884005479 Package: [10 Units] In Commercial Distribution |
GS1 | 50849884005474 [Package] Contains: 30849884005470 Package: [110 Units] In Commercial Distribution |
FOZ | Catheter, intravascular, therapeutic, short-term less than 30 days |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-02-09 |
Device Publish Date | 2023-02-01 |
38498840011929 | MARKED NITI/AU GUIDEWIRE, 0/018" X 130CM |
38498840011905 | MARKED NITINOL GUIDEWIRE, 0.018" X 80CM |
38498840012216 | 3.5F X 5CM PTFE TEARAWAY INTRODUCER |
38498840011912 | STAINLESS STEEL GUIDEWIRE, 0.018" X 80CM |
38498840011899 | NITI/AU GUIDEWIRE, 0.018" X 70CM |
38498840011882 | NITI/SS GUIDEWIRE, 0.018" X 45CM |
38498840011875 | MARKED NITI/AU GUIDEWIRE, 0.018" X 45CM |
38498840011813 | 5.5F X 10CM PTFE TEARAWAY INTRODUCER |
38498840011806 | 4.5F X 10CM PTFE TEARAWAY INTRODUCER |
38498840011790 | 6F X 7CM PTFE TEARAWAY INTRODUCER |
38498840011783 | 5.5F X 7CM PTFE TEARAWAY INTRODUCER |
38498840011776 | 4.0F X 7CM PTFE TEARAWAY INTRODUCER |
38498840011769 | 21GA. X 7CM INTRODUCER NEEDLE |
38498840011752 | 21GA. X 4CM INTRODUCER NEEDLE |
38498840011318 | 21GA SAFETY NEEDLE, 7CM |
38498840011301 | 21GA SAFETY NEEDLE, 4CM |
38498840012568 | ULTRASOUND IV START KIT |
38498840012230 | 4" MICROBORE EXTENSION SET |
38498840012223 | 3.5FR MST INSERTION KIT |
38498840012193 | CENTRAL LINE DRESSING KIT |
38498840011844 | 6.0FR MST INSERTION KIT |
38498840011837 | 5.5FR MST INSERTION KIT |
38498840011820 | 4.0FR MST INSERTION KIT |
38498840012537 | PREP KIT |
38498840012391 | PROCEDURE KIT |
38498840012384 | PICC INSERTION TRAY |
38498840012360 | VAD KIT W/ CHLORAPREP |
38498840012353 | VAD ACCESS KIT |
38498840012308 | VAD ACCESS KIT |
38498840012278 | VAD ACCESS TRAY |
38498840012254 | LEADERFLEX INSERTION KIT |
38498840011936 | PREP KIT |
38498840011677 | PROCEDURE TRAY |
38498840011646 | PIV INSERTION KIT |
38498840011363 | CENTRAL LINE KIT |
38498840011226 | CENTRAL VENOUS CATHETER KIT |
38498840011042 | PICC INSERTION TRAY |
38498840011035 | LEADERFLEX INSERTION KIT |
38498840010830 | LEADERFLEX INSERTION KIT |
38498840010663 | CENTRAL LINE KIT |
38498840010649 | PICC INSERTION TRAY |
38498840010632 | PICC INSERTION TRAY |
38498840010564 | NEONATAL PICC TRAY |
38498840010502 | CENTRAL LINE KIT |
38498840010496 | PICC/MIDLINE KIT |
38498840010151 | LEADERFLEX INSERTION TRAY |
38498840010144 | PICC LINE TRAY |
38498840010076 | INSERTION TRAY |
38498840010069 | MAXIMUM BARRIER TRAY |
38498840010007 | PICC INSERTION TRAY |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() VYGON 85083411 4021503 Live/Registered |
VYGON 2010-07-13 |
![]() VYGON 79340347 not registered Live/Pending |
VYGON 2022-03-29 |
![]() VYGON 79019449 3211611 Live/Registered |
VYGON 2005-11-14 |
![]() VYGON 76383231 2763518 Dead/Cancelled |
Vygon 2002-03-12 |