VisIV 1013303
GUDID 20887787001833
VisCap Port Cover For VisIV Container
HOSPIRA, INC.
Intravenous administration set| Primary Device ID | 20887787001833 |
| NIH Device Record Key | 5bfad516-bcb3-4499-8b60-201710e6b3f7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VisIV |
| Version Model Number | 1013303 |
| Catalog Number | 1013303 |
| Company DUNS | 141588017 |
| Company Name | HOSPIRA, INC. |
| Device Count | 150 |
| 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 |
Customer Support Contacts
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com | |
| Phone | +1(877)946-7747 |
| uscustomercare@pfizer.com |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
| Special Storage Condition, Specify | Between 0 and 0 *Adhere to storage requirements of added medications |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887787001839 [Unit of Use] |
| GS1 | 10887787001836 [Primary] |
| GS1 | 20887787001833 [Package] Contains: 10887787001836 Package: case [10 Units] In Commercial Distribution |
| HIBCC | M33510133030 [Secondary] |
FDA Product Code
| KPE | CONTAINER, I.V. |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-12-11 |
| Device Publish Date | 2016-12-02 |
Devices Manufactured by HOSPIRA, INC.
| M3351239104251 - Plum | 2022-07-04 PLUG n' PLAY MODULE |
| M3352079204251 - Plum | 2022-07-04 Plum A+ Version 13.43 w/MedNet |
| M3353001004051 - Plum 360 | 2022-07-04 PLUM 360 Infuser |
| 10887787001751 - MedNet | 2020-01-22 Metnet Software |
| 20887787001833 - VisIV | 2019-12-11VisCap Port Cover For VisIV Container |
| 20887787001833 - VisIV | 2019-12-11 VisCap Port Cover For VisIV Container |
| 20887787001871 - Additive | 2019-12-11 LATEX-FREE ADDITIVE HINGE CAP LifeCare Flexible Container |
| 20887787003011 - Plum | 2019-12-11 Primary PLUM Set Yellow Striped Tubing, Distal Microbore Tubing, Secure Lock, 107 Inch |
| 20887787003714 - Lifeshield | 2019-12-11 LIFESHIELD Extension Set, 5 Inch Prepierced T-Site with Spin Collar |
Trademark Results [VisIV]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VISIV 78872485 3295623 Live/Registered |
ICU MEDICAL, INC. 2006-04-28 |
 VISIV 78769599 3299628 Dead/Cancelled |
Hospira, Inc. 2005-12-08 |
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