| Primary Device ID | 07612964013656 |
| NIH Device Record Key | 77a77e5c-be9c-43da-8c96-774c89863c8e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DISPETTE® |
| Version Model Number | FH1705 |
| Catalog Number | FH1705 |
| Company DUNS | 483342734 |
| Company Name | Guest Scientific AG |
| 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 | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07612964013625 [Package] Package: INDIVIDUAL PACKAGING [1 Units] In Commercial Distribution |
| GS1 | 07612964013649 [Package] Package: BULK PACKAGING [20 Units] In Commercial Distribution |
| GS1 | 07612964013656 [Primary] |
| JPH | Test, Erythrocyte Sedimentation Rate |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-11-15 |
| Device Publish Date | 2019-11-07 |
| 07612964013656 | DISPETTE LEVELING STAND |
| 07612964013540 | DISPETTE PLUGGED |
| 07612964013410 | WINPETTE |
| 07612964013335 | DISPETTE ONE |
| 07612964013311 | DISPETTE 2 SALINE |
| 07612964000809 | DISPETTE 2 CITRATE |
| 07612964013113 | DISPETTE ONE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DISPETTE 86753390 4963604 Live/Registered |
Guest Scientific AG 2015-09-10 |
![]() DISPETTE 72259386 0842532 Dead/Expired |
AMERICAN CYANAMID COMPANY 1966-11-25 |