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 |
D0026077000 - Calibra® Abutment | 2024-05-03 Calibra® Abutment Resin Cement Syringe Refill |
D0026077010 - Calibra® Abutment | 2024-05-03 Calibra® Abutment Resin Cement Sample |
D0026690011 - SmartCem®2 Self-Adhesive Cement | 2024-05-03 SmartCem®2 Self-Adhesive Cement Syringe Introductory Kit |
D0026690031 - SmartCem®2 Self-Adhesive Cement | 2024-05-03 SmartCem®2 Self-Adhesive Cement Syringe Evaluator Kit |
D0026070711 - Calibra® Esthetic Resin Cement | 2024-05-02 Calibra® Esthetic Resin Cement, Try-In Paste, Light, 2 (1.8g) syringe Refill Package |
D0026070721 - Calibra® Esthetic Resin Cement | 2024-05-02 Calibra® Esthetic Resin Cement, Try-In Paste, Medium, 2 (1.8g) syringe Refill Package |
D0026070731 - Calibra® Esthetic Resin Cement | 2024-05-02 Calibra® Esthetic Resin Cement, Try-In Paste, Dark, 2 (1.8g) syringe Refill Package |
D0026070741 - Calibra® Esthetic Resin Cement | 2024-05-02 Calibra® Esthetic Resin Cement, Try-In Paste, Translucent, 2 (1.8g) syringe Refill Package |
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 |