| Primary Device ID | 10884521758995 |
| NIH Device Record Key | 1118f2c5-8ab3-474e-b9ce-f887a04ab709 |
| Commercial Distribution Discontinuation | 2018-03-26 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Zephyr |
| Version Model Number | 9607-0215 |
| Catalog Number | 9607-0215 |
| Company DUNS | 796678527 |
| Company Name | ZEPHYR TECHNOLOGY LLC |
| 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 | false |
| Serial Number | false |
| Manufacturing Date | true |
| 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(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.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 |
| Special Storage Condition, Specify | Between 0 and 0 *No; |
| Special Storage Condition, Specify | Between 0 and 0 *No; |
| Special Storage Condition, Specify | Between 0 and 0 *No; |
| Special Storage Condition, Specify | Between 0 and 0 *No; |
| Special Storage Condition, Specify | Between 0 and 0 *No; |
| Special Storage Condition, Specify | Between 0 and 0 *No; |
| Special Storage Condition, Specify | Between 0 and 0 *No; |
| Special Storage Condition, Specify | Between 0 and 0 *No; |
| Special Storage Condition, Specify | Between 0 and 0 *No; |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10884521758995 [Primary] |
| DRX | Electrode, electrocardiograph |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2021-03-10 |
| Device Publish Date | 2018-01-24 |
| 10884521758995 | Zephyr 5-Bay BioModule Charger For use with BH3 BioModule |
| 10884521758964 | Single Bay BioModule Charger |
| 90884521725467 | BioModule |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ZEPHYR 98590123 not registered Live/Pending |
Zephyr Dental Implant and Surgery Center 2024-06-07 |
![]() ZEPHYR 98201593 not registered Live/Pending |
ILONA, INC. 2023-09-28 |
![]() ZEPHYR 98144972 not registered Live/Pending |
Berner International 2023-08-22 |
![]() ZEPHYR 98124713 not registered Live/Pending |
Spall Lab Solutions LLC 2023-08-09 |
![]() ZEPHYR 98063556 not registered Live/Pending |
NoHo Zephyr, Inc. 2023-06-28 |
![]() ZEPHYR 97872934 not registered Live/Pending |
Southwick, Ryan 2023-04-04 |
![]() ZEPHYR 97708643 not registered Live/Pending |
Ford Motor Company 2022-12-08 |
![]() ZEPHYR 97398068 not registered Live/Pending |
Applied Materials, Inc. 2022-05-06 |
![]() ZEPHYR 97254081 not registered Live/Pending |
Channel Islands Management LLC 2022-02-04 |
![]() ZEPHYR 90687488 not registered Live/Pending |
Curbell Medical Products, Inc. 2021-05-03 |
![]() ZEPHYR 90660516 not registered Live/Pending |
Bell Sports, Inc. 2021-04-21 |
![]() ZEPHYR 90537322 not registered Live/Pending |
Yatsevich, Jason S. 2021-02-20 |