ANKYLOS® 31010130
GUDID 07392532215025
C/X Membrane Screw Ø 6.0 mm sinus lift 1 mm
Dentsply Implants Manufacturing GmbH
Dental implant suprastructure, permanent, preformed| Primary Device ID | 07392532215025 |
| NIH Device Record Key | 7113658d-cb18-4f44-8d4f-fcfc22a570c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ANKYLOS® |
| Version Model Number | 31010130 |
| Catalog Number | 31010130 |
| Company DUNS | 344038836 |
| Company Name | Dentsply Implants Manufacturing GmbH |
| 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 | true |
| 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 |
Customer Support Contacts
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Storage, in the original packaging, at room temperature in a dry place away from sunlight. |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07392532215025 [Primary] |
| HIBCC | EFRI310101302 [Previous] |
FDA Product Code
| DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
[07392532215025]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-03-15 |
| Device Publish Date | 2020-11-18 |
On-Brand Devices [ANKYLOS®]
| EFRI310563042 | Horizontal screw seat for fixation screw M1.4 |
| EFRI310563012 | Fixation Screw Lateral Hexagon M1.4 |
| EFRI310562702 | Splinting Screw for Individual Screw Retention, long |
| EFRI310562602 | Splinting Screw for Individual Screw Retention, medium |
| EFRI310562502 | Splinting Screw for Individual Screw Retention, short |
| EFRI310562182 | Titanium coping Balance Base abutment narrow |
| EFRI310562172 | Retention Coping long for Balance Base Abutment narrow |
| EFRI310562162 | Retention coping Balance Base abutment narrow |
| EFRI310562152 | Retention Coping for Balance Base Abutment |
| EFRI310562122 | Gold Coping Balance Base abutment narrow (Permador® PDF) |
| EFRI310562102 | Gold Coping for Balance Base Abutment (Degunorm) with screw |
| EFRI310562002 | Gold Coping for Balance Base Abutment (Permador PDF) with screw |
| EFRI310561902 | Gold Coping, Degunorm b/1.5/6.0 & b/3.0/6.0 with screw |
| EFRI310561802 | Gold Coping, Degunorm b/1.5/4.0 & b/3.0/4.0 with screw |
| EFRI310561702 | Gold Coping, Degunorm a/1.5/6.0 & a/3.0/6.0 with screw |
| EFRI310561602 | Gold Coping, Degunorm a/1.5/4.0 & a/3.0/4.0 with screw |
| EFRI310561402 | Screw for Gold Coping |
| EFRI310561302 | Gold Coping, Permador b/1.5/6.0 & b/3.0/6.0 with screw |
| EFRI310561202 | Gold Coping, Permador b/1.5/4.0 & b/3.0/4.0 with screw |
| EFRI310561102 | Gold Coping, Permador a/1.5/6.0 & a/3.0/6.0 with screw |
| EFRI310561002 | Gold Coping, Permador a/1.5/4.0 & a/3.0/4.0 with screw |
| EFRI310560542 | Retaining Screw, lateral hexagon M1.2 |
| EFRI310560522 | Sleeve for retaining screw, lateral hexagon |
| EFRI310560512 | Retaining Screw, lateral hexagon M1x0.2 |
| EFRI310560262 | Fixation Screw, occlusal M1.6 mm Hex, L19 mm |
| EFRI310560252 | Fixation Screw, occlusal M1.6 mm Hex, extra long |
| EFRI310560242 | Fixation Screw, occlusal M1.6 mm Hex, long |
| EFRI310560222 | Fixation Screw, occlusal M1.6 mm Hex |
| EFRI310560212 | Retaining Screw, occlusal hexagon M1.6 |
| EFRI310560102 | Headless Screw |
| EFRI310452132 | Wax-Up Screw, long |
| EFRI310452112 | Wax-Up Screw, short |
| EFRI310241832 | Regular C/ Abutment GH4.5/A22.5 |
| EFRI310241822 | Regular C/ Abutment GH4.5/A15 |
| EFRI310241812 | Regular C/ Abutment GH4.5/A7.5 |
| EFRI310241802 | Regular C/ Abutment GH4.5/A0 |
| EFRI310241732 | Regular C/ Abutment GH3.0/A22.5 |
| EFRI310241722 | Regular C/ Abutment GH3.0/A15 |
| EFRI310241712 | Regular C/ Abutment GH3.0/A7.5 |
| EFRI310241702 | Regular C/ Abutment GH3.0/A0 |
| EFRI310241632 | Regular C/ Abutment GH1.5/A22.5 |
| EFRI310241622 | Regular C/ Abutment GH1.5/A15 |
| EFRI310241612 | Regular C/ Abutment GH1.5/A7.5 |
| EFRI310241602 | Regular C/ Abutment GH1.5/A0 |
| EFRI310241532 | Regular C/ Abutment GH0.75/A22.5 |
| EFRI310241522 | Regular C/ Abutment GH0.75/A15 |
| EFRI310241512 | Regular C/ Abutment GH0.75/A7.5 |
| EFRI310241502 | Regular C/ Abutment GH0.75/A0 |
| EFRI310241432 | Regular /X Abutment GH4.5/A22.5 |
| EFRI310241422 | Regular /X Abutment GH4.5/A15 |
Trademark Results [ANKYLOS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ANKYLOS 74688199 2079843 Live/Registered |
DEGUDENT GMBH 1995-06-14 |
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