| Primary Device ID | 14931921878559 |
| NIH Device Record Key | 8cb2e24a-6740-4be4-ab95-8d3b25e68eed |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BluPRO® |
| Version Model Number | TL-272T3 |
| Catalog Number | TL-272T3 |
| Company DUNS | 690568050 |
| Company Name | NIHON KOHDEN CORPORATION |
| Device Count | 24 |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com | |
| Phone | +1(800)325-0283 |
| info@nkusa.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04931921878552 [Unit of Use] |
| GS1 | 14931921878559 [Primary] |
| MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) |
| 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 | 2016-09-05 |
| 04931921877494 | Finger probe Adult, child (20 kg or more) Finger or toe |
| 04931921877432 | Finger probe Adult, child (20 kg or more) Finger or toe |
| 04931921871188 | Multi-site probe Adults, child (3 kg or more) |
| 04931921852712 | Finger probe Adult, child (20kg or more) Finger |
| 14931921878597 | SpO2 probe Child / Infant (from 3 to 20 kg) Finger or toe, disposable |
| 14931921878573 | SpO2 probe Adults (40 kg or more) Finger or toe, disposable |
| 14931921878559 | SpO2 probe Child (from 10 to 50 kg) Finger or toe, disposable |
| 14931921878535 | SpO2 probe Adults (30 kg or more) Finger or toe, disposable |
| 14931921874308 | SpO2 Probe Infant (from 3 to 20 kg) finger or toe, disposable |
| 14931921874285 | SpO2 probe Neonate (less than 3kg) instep, Adults (40 kg or more) Finger or toe, disposable |
| 14931921874261 | SpO2 probe Child (from 10 to 50 kg) Finger or toe, disposable |
| 14931921874247 | SpO2 probe Adults (30 kg or more) Finger or toe, disposable |
| 14931921863357 | SpO2 Probe, multi-site Y probe, disposable |
| 04931921005828 | SpO2 probe Adults (30 kg or more) Finger or toe, disposable |