| Primary Device ID | 40072000758357 |
| NIH Device Record Key | 96b812d2-03c9-476e-a2aa-5c47f7d686f5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Guaranteed Quality Products |
| Version Model Number | KD-120 |
| Company DUNS | 131978533 |
| Company Name | KMART HOLDING CORPORATION |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | 303-271-0300 |
| info@180innovations.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00072000758359 [Primary] |
| GS1 | 20072000758353 [Package] Contains: 00072000758359 Package: inner carton [6 Units] In Commercial Distribution |
| GS1 | 40072000758357 [Package] Contains: 20072000758353 Package: case [24 Units] In Commercial Distribution |
| FLL | Thermometer, Electronic, Clinical |
| 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 | 2016-09-20 |
| 40072000783892 | A hand-held, battery-powered, electronic instrument designed for oral, under arm or rectal use t |
| 00072000764978 | A hand-held, battery-powered, electronic instrument designed for oral, under arm or rectal use t |
| 40072000758357 | A hand-held, battery-powered, electronic instrument designed for oral, under arm or rectal use t |