Primary Device ID | 50085412565625 |
NIH Device Record Key | a461155b-225e-4950-860f-6b8635fd4d99 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 2R1145 |
Catalog Number | 2R1145 |
Company DUNS | 005146311 |
Company Name | BAXTER INTERNATIONAL INC. |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM | |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00085412565620 [Primary] |
GS1 | 50085412565625 [Package] Contains: 00085412565620 Package: CASE [48 Units] In Commercial Distribution |
FPA | Set, administration, intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-12-11 |
Device Publish Date | 2019-03-29 |
50085412676628 - CLR1 - CLEARLINK | 2023-07-24 Non-DEHP Solution Set, Luer Activated Valve, Male Luer Lock Adapter with Retractable Collar, 100” (2.5m) approx., 10 drops/mL |
50085412002335 - INTERLINK | 2020-06-30 Extension Set, Injection Site, Male Luer Lock Adapter with Retractable Collar |
50085412031199 - INTERLINK | 2020-06-30 Y-Type Blood/Solution Set, 40 and 150 Micron Dual Screen Filter, Injection Site, Male Luer Lock Adapter with Retractable Collar |
50085412065293 - INTERLINK | 2020-06-30 Y-Type Blood/Solution Set with 40 and 150 Micron Dual Screen Filter and Pressure Pump, Injection Site, Male Luer Lock Adapter wi |
50085412046162 - NA | 2020-05-06 Evacuated Container, 1000 mL |
50085412565625 - NA | 2019-12-11Non-DEHP IV Fat Emulsion Administration Set, Male Luer Lock Adapter with Retractable Collar |
50085412565625 - NA | 2019-12-11 Non-DEHP IV Fat Emulsion Administration Set, Male Luer Lock Adapter with Retractable Collar |
50085412565946 - NA | 2019-12-11 Non-DEHP IV Fat Emulsion Administration Set, Male Luer Lock Adapter with Retractable Collar |
50085412000522 - INTERLINK/CONTINU-FLO | 2019-12-11 Non-DEHP CONTINU-FLO Solution Set, 2 Injection Sites, Male Luer Lock Adapter with Retractable Collar |