| Primary Device ID | 00845275004991 |
| NIH Device Record Key | d6dc4df9-1f66-4bd7-b22f-d0df4adbf7ea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Thermo Scientific Protocol™ Parasitology System |
| Version Model Number | 23-005-33 |
| Company DUNS | 183998769 |
| Company Name | Fisher Diagnostics |
| Device Count | 20 |
| 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 |
| Phone | 800-528-0494 |
| xx@xx.xx |
| Storage Environment Temperature | Between 15 Degrees Celsius and 30 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00845275004991 [Primary] |
| GS1 | 00845275006377 [Unit of Use] |
| LDZ | Fixative, Alcohol Containing |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-16 |
| 00845275005134 | 23-005-68 |
| 00845275005127 | 23-005-51 |
| 00845275005110 | 23-005-50 |
| 00845275005103 | 23-005-47 |
| 00845275005097 | 23-005-46 |
| 00845275005080 | 23-005-45 |
| 00845275005073 | 23-005-44 |
| 00845275005066 | 23-005-43 |
| 00845275005042 | 23-005-41 |
| 00845275005035 | 23-005-40 |
| 00845275005028 | 23-005-39 |
| 00845275005011 | 23-005-38 |
| 00845275005004 | 23-005-37 |
| 00845275004991 | 23-005-33 |
| 00845275004984 | 23-005-32 |
| 00845275004977 | 23-005-31 |
| 00845275004960 | 23-005-30 |
| 00845275004953 | 23-005-28 |
| 00845275004946 | 23-005-27 |
| 00845275004939 | 23-005-26 |