| Primary Device ID | 30884521554256 |
| NIH Device Record Key | 9a2ca200-e4e9-4ec2-8024-ad97dd09aaca |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | non branded |
| Version Model Number | 9051 |
| Catalog Number | 9051 |
| Company DUNS | 080935429 |
| Company Name | Cardinal Health, Inc. |
| Device Count | 10 |
| 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 | false |
| 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(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com |
| Length | 90 Feet |
| Width | 2 Inch |
| Length | 90 Feet |
| Width | 2 Inch |
| Special Storage Condition, Specify | Between 0 and 0 *; |
| Special Storage Condition, Specify | Between 0 and 0 *; |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20884521554259 [Primary] |
| GS1 | 30884521554256 [Package] Contains: 20884521554259 Package: CASE [100 Units] In Commercial Distribution |
| GS1 | 40884521554253 [Unit of Use] |
| DSF | RECORDER, PAPER CHART |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-02-15 |
| Device Publish Date | 2018-06-27 |
| 30884521554256 | Medical Recording Chart Paper |
| 20884521554228 | Medical Recording Chart Paper |
| 10884521554290 | Medical Recording Chart Paper |
| 10884521554481 | Medical Recording Chart Paper |