| Primary Device ID | 06902139111593 |
| NIH Device Record Key | 75a2077e-6095-4b81-a39d-d19308902108 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Reverse Awl |
| Version Model Number | 110301800 |
| Catalog Number | 110301800 |
| Company DUNS | 529366055 |
| Company Name | Double Medical Technology 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 | +865926087101 |
| info@double-medical.com | |
| Phone | +865926087101 |
| info@double-medical.com | |
| Phone | +865926087101 |
| info@double-medical.com | |
| Phone | +865926087101 |
| info@double-medical.com | |
| Phone | +865926087101 |
| info@double-medical.com | |
| Phone | +865926087101 |
| info@double-medical.com | |
| Phone | +865926087101 |
| info@double-medical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06902139111593 [Primary] |
| HSB | Rod, Fixation, Intramedullary And Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[06902139111593]
Moist Heat or Steam Sterilization
[06902139111593]
Moist Heat or Steam Sterilization
[06902139111593]
Moist Heat or Steam Sterilization
[06902139111593]
Moist Heat or Steam Sterilization
[06902139111593]
Moist Heat or Steam Sterilization
[06902139111593]
Moist Heat or Steam Sterilization
[06902139111593]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-01 |