| Primary Device ID | 07612964013540 |
| NIH Device Record Key | d6533f98-8b80-43a2-9069-c530df2dffeb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DISPETTE® |
| Version Model Number | FH1530 |
| Catalog Number | FH1530 |
| Company DUNS | 483342734 |
| Company Name | Guest Scientific AG |
| Device Count | 250 |
| 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 | 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 | 07612964013533 [Primary] |
| GS1 | 07612964013540 [Package] Contains: 07612964013533 Package: CASE [10 Units] In Commercial Distribution |
| GS1 | 07612964013557 [Unit of Use] |
| 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 |