Primary Device ID | 03660812125390 |
NIH Device Record Key | 9865f55f-0534-44f4-bff7-52483806faa2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VYGON |
Version Model Number | 1212.04 |
Catalog Number | 00121204 |
Company DUNS | 315994731 |
Company Name | VYGON-Erzeugnisse für Medizin und Chirurgie-GmbH und Co. KG |
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 |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03660812125390 [Primary] |
FOZ | Catheter, intravascular, therapeutic, short-term less than 30 days |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-06 |
Device Publish Date | 2023-08-29 |
33660812082236 | Nutriline |
33660812075382 | EPICUTANEO PUR |
33660812039230 | Leaderflex 22G (0,7mm x 60mm) 22G |
33660812011311 | Leaderflex 22G 0,5x0,7mmx200mm |
33660812011304 | Leaderflex 22G (0,7mm x 80mm) 22G |
33660812011298 | Leaderflex 22G (0,7mm x 40mm) 22G |
33660812124493 | Extension set for ECC |
53660812138715 | premicath Ø0.35mmx200mm 28G 1Fr - Catheter with stylet and splitting needle |
53660812125470 | leaderflex 0.55mmx0.75mmx200mm 22G - 1 lumen catheter set |
53660812125432 | leaderflex 0.55mmx0.75mmx80mm 22G - 1 lumen catheter set |
53660812125401 | leaderflex 0.55mmx0.75mmx60mm 22G - 1 lumen catheter set |
33660812151604 | epicutaneo cava - Catheter with winged needle (0,3x0,6mmx150mm) 24G (2Fr) |
53660812151592 | epicutaneo cava - Catheter with winged needle (0,3x0,6mmx500mm) 24G (2Fr) |
03660812125390 | Leaderflex 22G (0,7mm x 40mm) |
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 |