| Primary Device ID | 00860002676401 |
| NIH Device Record Key | 0ad6aed4-4ae4-4481-8a73-5d3a154443ef |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ExoShield |
| Version Model Number | 40010548 |
| Catalog Number | 40010548 |
| Company DUNS | 025677872 |
| Company Name | NORTHSTAR MEDICAL RADIOISOTOPES, LLC |
| Device Count | 1 |
| 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 | false |
| Lot Batch | false |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860002676401 [Primary] |
| EAK | Screen, Leaded, Operator Radiation Protector |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-01-15 |
| Device Publish Date | 2020-01-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() EXOSHIELD 90330336 not registered Live/Pending |
Tape Specialists of Florida, Inc. 2020-11-19 |
![]() EXOSHIELD 88463549 not registered Live/Pending |
Neverfrost Inc. 2019-06-07 |
![]() EXOSHIELD 87720942 5529035 Live/Registered |
Nova USA Wood Products LLC 2017-12-14 |
![]() EXOSHIELD 87589530 not registered Live/Pending |
ThreeBond Co., Ltd. 2017-08-30 |
![]() EXOSHIELD 87310489 not registered Dead/Abandoned |
Nova USA Wood Products LLC 2017-01-23 |
![]() EXOSHIELD 77854087 3951760 Live/Registered |
REYEWEAR ACQUISITION, INC. 2009-10-21 |
![]() EXOSHIELD 77174609 3459104 Dead/Cancelled |
Michael Katsanevas 2007-05-07 |