Primary Device ID | 00850030354419 |
NIH Device Record Key | c1166485-3172-470e-9115-e8627a89163a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HydroMID |
Version Model Number | 90004104 |
Catalog Number | 90004104 |
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 | 00850030354419 [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 | 2024-06-12 |
Device Publish Date | 2024-06-04 |
00862559000449 | Midline catheter |
00850030354419 | Marked Midline Catheter (Mobile Kit) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() HYDROMID 90229032 not registered Live/Pending |
Access Vascular, Inc. 2020-10-01 |