| Primary Device ID | 00883205003799 |
| NIH Device Record Key | bf236c00-b4a2-4545-bae7-45a9194a8270 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ultrapak |
| Version Model Number | 133 |
| Catalog Number | 133 |
| Company DUNS | 013369913 |
| Company Name | ULTRADENT PRODUCTS, INC. |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com | |
| Phone | +1(801)572-4200 |
| customerservice@ultradent.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00883205003799 [Primary] |
| JES | FLOSS, DENTAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-05-29 |
| Device Publish Date | 2018-04-28 |
| 00883205003829 | Ultrapak Cord Kit |
| 00883205003812 | Ultrapak Cord #0 |
| 00883205003805 | Ultrapak Cord #1 |
| 00883205003799 | Ultrapak Cord #2 |
| 00883205003782 | Ultrapak Cord #3 |
| 00883205003768 | Ultrapak Cord #00 |
| 00883205003751 | Ultrapak Cord #000 |
| 00883205031778 | Sample Cord Ultradent |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ULTRAPAK 98892106 not registered Live/Pending |
Ascend Eagle Inc 2024-12-09 |
![]() ULTRAPAK 98616185 not registered Live/Pending |
Gravel, LLC 2024-06-24 |
![]() ULTRAPAK 88466388 not registered Live/Pending |
DADCO, Inc. 2019-06-11 |
![]() ULTRAPAK 86340074 4815988 Live/Registered |
uNu Electronics, Inc. 2014-07-17 |
![]() ULTRAPAK 85901332 4439788 Live/Registered |
Interstate Group Holdings, Inc. 2013-04-11 |
![]() ULTRAPAK 80991328 0991328 Dead/Cancelled |
Gould Inc. 0000-00-00 |
![]() ULTRAPAK 78767839 not registered Dead/Abandoned |
JL Industries 2005-12-06 |
![]() ULTRAPAK 78375224 3298733 Dead/Cancelled |
DADCO, Inc. 2004-02-27 |
![]() ULTRAPAK 77894790 not registered Dead/Abandoned |
Harleysville Mutual Insurance Company 2009-12-16 |
![]() ULTRAPAK 77165879 3365118 Dead/Cancelled |
JL Industries, Inc. 2007-04-25 |
![]() ULTRAPAK 75218159 2162877 Live/Registered |
HERAEUS NOBLELIGHT AMERICA LLC 1996-12-13 |
![]() ULTRAPAK 75059625 2117353 Dead/Cancelled |
INTERSTATE 1996-02-20 |