Primary Device ID | 07612964013113 |
NIH Device Record Key | 26ccdae0-431b-4315-b23b-c953a708d27c |
Commercial Distribution Discontinuation | 2021-06-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | DISPETTE® |
Version Model Number | FH1500 |
Catalog Number | FH1500 |
Company DUNS | 483342734 |
Company Name | Guest Scientific AG |
Device Count | 100 |
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 | 07612964013106 [Primary] |
GS1 | 07612964013113 [Package] Contains: 07612964013106 Package: CASE [10 Units] Discontinued: 2021-06-30 Not in Commercial Distribution |
GS1 | 07612964013120 [Unit of Use] |
JPH | Test, Erythrocyte Sedimentation Rate |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2021-10-20 |
Device Publish Date | 2020-06-01 |
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 |