| Primary Device ID | 20887787001819 |
| NIH Device Record Key | fe55f504-5adb-413a-9ba0-15ea87c30d84 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nutri-Clamp |
| Version Model Number | 791501 |
| Catalog Number | 0791501 |
| Company DUNS | 141588017 |
| Company Name | HOSPIRA, INC. |
| Device Count | 50 |
| 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 | false |
| 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(877)946-7747 |
| uscustomercare@pfizer.com |
| Special Storage Condition, Specify | Between 0 and 0 *Do not store at extreme temperatures |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887787001815 [Unit of Use] |
| GS1 | 10887787001812 [Primary] |
| GS1 | 20887787001819 [Package] Contains: 10887787001812 Package: case [8 Units] In Commercial Distribution |
| HIBCC | M3357915011 [Secondary] |
| KPE | CONTAINER, I.V. |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2016-12-02 |
| 20887787001826 | NUTRI-CLAMP Closure Device for use with Hospira Heavy Dextrose Partial-Fill Containers |
| 20887787001819 | NUTRI-CLAMP Closure Device for use with Hospira Empty Containers with Attached Transfer Set |
| 20887787001802 | NUTRI-CLAMP Closure Device FOR USE WITH NUTRIMIX-MACRO EMPTY CONTAINER WITH ATTACHED TRANSFER SE |