| Primary Device ID | 10860802000366 |
| NIH Device Record Key | 5f9378d2-c172-4d59-9070-b0fddeb6df53 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 903™ |
| Version Model Number | W181 |
| Company DUNS | 079861573 |
| Company Name | EASTERN BUSINESS FORMS INC |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860802000369 [Primary] |
| GS1 | 10860802000366 [Package] Contains: 00860802000369 Package: [7200 Units] In Commercial Distribution |
| JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-01-21 |
| Device Publish Date | 2018-12-21 |
| 10860802000366 | 903 Filter Paper |
| 00860802000352 | 903 Filter Paper |
| 10860802000342 | 903 Filter Paper |
| 00860802000338 | 903 Filter Paper |
| 10860802000373 | 903 Filter Paper |
| 10860802000380 | 903 Filter Paper |
| 00850039198014 | 903 Filter Paper Lot#-variable |
| 00850039198007 | 903 Filter Paper |
| 10850039198028 | W221 |
| 10850039198042 | W231 |