DUAFIT A60 SP106
GUDID 03760225718735
DUAFIT PIP 10° PEEK STERILE SIZE 2L
IN2BONES
Interphalangeal joint arthrodesis implant| Primary Device ID | 03760225718735 |
| NIH Device Record Key | a3f067ca-08f0-46e6-a210-c08367f283a3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DUAFIT |
| Version Model Number | A60 SP106 |
| Catalog Number | A60 SP106 |
| Company DUNS | 263616749 |
| Company Name | IN2BONES |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03760225718735 [Primary] |
FDA Product Code
| HWC | Screw, fixation, bone |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-23 |
| Device Publish Date | 2024-12-13 |
On-Brand Devices [DUAFIT]
| 03760225712993 | A06 10401 |
| 03760225718759 | DUAFIT PIP 17° PEEK STERILE SIZE 2L |
| 03760225718742 | DUAFIT PIP 17° PEEK STERILE SIZE 1L |
| 03760225718735 | DUAFIT PIP 10° PEEK STERILE SIZE 2L |
| 03760225718728 | DUAFIT PIP 10° PEEK STERILE SIZE 1L |
| 03701337603052 | DUAFIT PIP 0° PEEK STERILE SIZE 2L |
| 03701337603045 | DUAFIT PIP 0° PEEK STERILE SIZE 1L |
Trademark Results [DUAFIT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DUAFIT 79158925 4762598 Live/Registered |
In2Bones 2014-07-29 |
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