Primary Device ID | 50085412025365 |
NIH Device Record Key | 69540e44-a99f-4488-9a49-15f26a1f0f57 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 5C4527 |
Catalog Number | 5C4527 |
Company DUNS | 005083209 |
Company Name | BAXTER HEALTHCARE CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 | false |
OTC Over-The-Counter | true |
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 | |
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 | 00085412025360 [Primary] |
GS1 | 50085412025365 [Package] Contains: 00085412025360 Package: CASE [12 Units] In Commercial Distribution |
FKK | CLAMP, LINE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-25 |
Device Publish Date | 2019-03-15 |
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