Primary Device ID | 30841156100821 |
NIH Device Record Key | 63ced279-e648-4611-9f99-64cf06d036f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VENTURE |
Version Model Number | IPN913590 |
Catalog Number | 5823 |
Company DUNS | 002348191 |
Company Name | TELEFLEX INCORPORATED |
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 | true |
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 |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM |
Length | 120 Centimeter |
Length | 120 Centimeter |
Length | 120 Centimeter |
Length | 120 Centimeter |
Length | 120 Centimeter |
Length | 120 Centimeter |
Length | 120 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10841156100827 [Primary] |
GS1 | 30841156100821 [Package] Contains: 10841156100827 Package: Box [1 Units] In Commercial Distribution |
DQY | Catheter, percutaneous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-11 |
Device Publish Date | 2019-01-22 |
20841156102248 | Venture OTW |
20841156102231 | Venture RX |
30841156100838 | Venture 038 70cm |
30841156100821 | Venture 038 120cm |
20841156106529 | Venture .014 RX |
20841156106512 | Venture .014 OTW |