Primary Device ID | 00850030354310 |
NIH Device Record Key | 56b3a707-0819-49aa-9a3c-893f22a91716 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HydroPICC Dual Lumen |
Version Model Number | 80H02101 |
Catalog Number | 80H02101 |
Company DUNS | 085539114 |
Company Name | ACCESS VASCULAR, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850030354310 [Primary] |
LJS | Catheter, Intravascular, Therapeutic, Long-Term Greater 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 | 2023-12-27 |
Device Publish Date | 2023-12-19 |
00850030354068 | HydroPICC Dual Lumen – Maximal Barrier Kit |
00850030354044 | HydroPICC 5Fr Dual Lumen Basic Kit (80cm GW) |
00850030354037 | HydroPICC 5Fr Dual Lumen Basic Kit (130cm GW) |
00850030354273 | HydroPICC Marked 5Fr Dual Lumen Maximal Barrier Kit |
00850030354266 | HydroPICC Marked 5Fr Dual Lumen Basic Kit (80cm GW) |
00850030354259 | HydroPICC Marked 5Fr Dual Lumen Basic Kit (130cm GW) |
00850030354334 | HydroPICC Marked 5Fr Dual Lumen Maximal Barrier Kit |
00850030354327 | HydroPICC Marked 5Fr Dual Lumen Basic Kit (70cm GW) |
00850030354310 | HydroPICC Marked 5Fr Dual Lumen Basic Kit (130cm GW) |
00850030354402 | 5F Dual Lumen Peripherally Inserted Central Marked Catheter (Mobile Kit) |