| Primary Device ID | 30849884000017 |
| NIH Device Record Key | c42689ae-9a95-42cb-b0a3-779dc305c9ee |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VYGON |
| Version Model Number | AMS-656 |
| Catalog Number | AMS-656 |
| 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 | 00849884000016 [Primary] |
| GS1 | 30849884000017 [Package] Contains: 00849884000016 Package: [100 Units] In Commercial Distribution |
| FPA | Set, administration, intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-11-11 |
| Device Publish Date | 2019-11-01 |
| 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 |