| Primary Device ID | D002625130102 |
| NIH Device Record Key | ae37103c-6218-49fd-b756-634283b4d224 |
| Commercial Distribution Discontinuation | 2018-12-05 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Hydrosil® Hydromonophase Vinyl Polysiloxane Impression Material |
| Version Model Number | 625130 |
| Catalog Number | 625130 |
| Company DUNS | 083235549 |
| Company Name | DENTSPLY INTERNATIONAL INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 90 Milliliter |
| Device Size Text, specify | 0 |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of direct sunlight. |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D0026251301 [Primary] |
| HIBCC | D002625130102 [Package] Contains: D0026251301 Package: Box [10 Units] Discontinued: 2018-12-03 Not in Commercial Distribution |
| ELW | MATERIAL, IMPRESSION |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-01-30 |
| Device Publish Date | 2016-09-21 |
| D0013011311 - Ceramco® 3 | 2026-02-17 |
| D0013011321 - Ceramco® 3 | 2026-02-17 |
| D0013011351 - Ceramco® 3 | 2026-02-17 |
| D0013011361 - Ceramco® 3 | 2026-02-17 |
| D0013011381 - Ceramco® 3 | 2026-02-17 |
| D0013011401 - Ceramco® 3 | 2026-02-17 |
| D0013011411 - Ceramco® 3 | 2026-02-17 |
| D0013011421 - Ceramco® 3 | 2026-02-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HYDROSIL 86682330 not registered Dead/Abandoned |
Quest Construction Products, LLC 2015-07-02 |
![]() HYDROSIL 86350777 not registered Dead/Abandoned |
Rochester Medical Corporation 2014-07-29 |
![]() HYDROSIL 80996221 0996221 Dead/Cancelled |
J. M. Huber Corporation 0000-00-00 |
![]() HYDROSIL 78547149 not registered Dead/Abandoned |
DEGUSSA CORPORATION 2005-01-13 |
![]() HYDROSIL 76196377 not registered Dead/Abandoned |
DEGUSSA CORPORATION 2001-01-18 |
![]() HYDROSIL 75737136 not registered Dead/Abandoned |
Polymer Technology Group Inc, The 1999-06-25 |
![]() HYDROSIL 74170409 not registered Dead/Abandoned |
Unimin Specialty Minerals, Inc. 1991-05-28 |
![]() HYDROSIL 74062182 1806635 Live/Registered |
Huls America Inc. 1990-05-24 |
![]() HYDROSIL 73669307 1475618 Live/Registered |
DENTSPLY INTERNATIONAL INC. 1987-06-29 |
![]() HYDROSIL 73315130 1195074 Dead/Cancelled |
American Sterilizer Company 1981-06-17 |