| Primary Device ID | 07333066011097 |
| NIH Device Record Key | 9bf1b50c-393b-4783-ac39-809b160163ef |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Development Solution |
| Version Model Number | 34-2232-63 |
| Catalog Number | 34-2232-63 |
| 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 |
| Special Storage Condition, Specify | Between 0 and 0 *Do not freeze! |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07333066011097 [Primary] |
| DHB | SYSTEM, TEST, RADIOALLERGOSORBENT (RAST) IMMUNOLOGICAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |
| 07333066011097 | Development Solution |
| 07333066000176 | Development Solution |
| 07333066000640 | Development Solution |
| 07333066000442 | Development Solution |
| 07333066000435 | Development Solution |