Primary Device ID | 50085412656026 |
NIH Device Record Key | 2143c05f-60fc-4376-a334-a93757dded14 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MiniCap |
Version Model Number | EZPC4466 |
Catalog Number | EZPC4466 |
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 | 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)933-0303 |
MEDINFO_MEDPRODUCTS@BAXTER.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00085412656021 [Primary] |
GS1 | 50085412656026 [Package] Contains: 00085412656021 Package: CASE [60 Units] In Commercial Distribution |
KDJ | SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-30 |
Device Publish Date | 2019-07-22 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MINICAP 98504498 not registered Live/Pending |
Minicap LLC 2024-04-17 |
MINICAP 88192226 5780722 Live/Registered |
Athena GTX, Inc. 2018-11-13 |
MINICAP 77979196 4092761 Live/Registered |
Sebia 2008-12-23 |
MINICAP 77638950 3858787 Live/Registered |
Sebia 2008-12-23 |
MINICAP 76664043 3458565 Live/Registered |
EATON TECHNOLOGIES GMBH 2006-08-02 |
MINICAP 75532774 not registered Dead/Abandoned |
Thatcher Tubes LLC 1998-08-07 |
MINICAP 74574949 not registered Dead/Abandoned |
JOHNSON & JOHNSON 1994-09-19 |
MINICAP 74162155 1707951 Dead/Cancelled |
Mine Safety Appliances Company 1991-04-29 |