| Primary Device ID | 08714729892038 |
| NIH Device Record Key | cf92be03-20e5-44ec-abe6-6a322d191a21 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NovaGold |
| Version Model Number | 5200 |
| Company DUNS | 868303074 |
| Company Name | HERAEUS MEDICAL COMPONENTS 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | 08714729854418 [Package] Package: Box [2 Units] In Commercial Distribution |
| GS1 | 08714729892038 [Primary] |
| OCY | Endoscopic Guidewire, Gastroenterology-Urology |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2021-08-24 |
| Device Publish Date | 2016-09-21 |
| 08714729892045 | 5201 |
| 08714729892038 | 5200 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NOVAGOLD 85962373 4574621 Live/Registered |
Novagold Resources Inc. 2013-06-18 |
![]() NOVAGOLD 85821491 4602231 Live/Registered |
Boston Scientific Scimed, Inc. 2013-01-11 |
![]() NOVAGOLD 75822400 not registered Dead/Abandoned |
Novamed Medical Products Manufacturing,Inc. 1999-10-14 |
![]() NOVAGOLD 74732084 not registered Dead/Abandoned |
NOVAMED MEDICAL PRODUCTS MANUFACTURING,INC. 1995-09-21 |