Primary Device ID | 51978860004367 |
NIH Device Record Key | e64bda2e-19dd-430d-84bc-2313cf495731 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CLEARLINK/CONTINU-FLO |
Version Model Number | ALT2402 |
Catalog Number | ALT2402 |
Company DUNS | 005083209 |
Company Name | BAXTER HEALTHCARE 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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com | |
Phone | +1(800)933-0303 |
US-MEDINFO_MEDPRODUCTS@baxter.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 01978860004362 [Primary] |
GS1 | 51978860004367 [Package] Contains: 01978860004362 Package: Case [48 Units] In Commercial Distribution |
FPA | Set, administration, intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-04 |
Device Publish Date | 2024-03-27 |
51978860004367 | QuickStay Set, 24 Hour Max Use, For Gravity Use Only, Clearlink System, Non-DEHP Continu-Flo Sol |
51978860004350 | QuickStay Set, 24 Hour Max Use, For Gravity Use Only, Clearlink System, Non-DEHP Continu-Flo Sol |
50197886004361 | QuickStay Set, 24 Hour Max Use, For Gravity Use Only, Clearlink System, Non-DEHP Continu-Flo Sol |
50197886004354 | QuickStay Set, 24 Hour Max Use, For Gravity Use Only, Clearlink System, Non-DEHP Continu-Flo Sol |