| Primary Device ID | 07333066000435 |
| NIH Device Record Key | 250a277a-791b-49b2-ab36-b531bf99d1e8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Development Solution |
| Version Model Number | 34-2329-01 |
| Catalog Number | 34-2329-01 |
| Company DUNS | 354019424 |
| Company Name | Phadia AB |
| Device Count | 1 |
| 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 | false |
| 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 | +469999999999 |
| xx@xx.xx |
| Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07333066000435 [Package] Contains: 07333066019895 Package: [6 Units] In Commercial Distribution |
| GS1 | 07333066019895 [Primary] |
| DHB | System, test, radioallergosorbent (rast) immunological |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-08 |
| Device Publish Date | 2019-03-29 |
| 07333066011097 | Development Solution |
| 07333066000176 | Development Solution |
| 07333066000640 | Development Solution |
| 07333066000442 | Development Solution |
| 07333066000435 | Development Solution |