| Primary Device ID | 06902139111791 |
| NIH Device Record Key | 62567a17-3d2b-4bab-9025-0a1aec78ed65 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Drill Guide for Guide Wire |
| Version Model Number | 110303900 |
| Catalog Number | 110303900 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06902139111791 [Primary] |
| HSB | Rod, Fixation, Intramedullary And Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[06902139111791]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-04-06 |
| Device Publish Date | 2016-09-01 |
| 06902139111791 - Drill Guide for Guide Wire | 2020-04-06 |
| 06902139111791 - Drill Guide for Guide Wire | 2020-04-06 |
| 06902139111982 - T-Handle with Quick Coupling | 2020-04-06 |
| 06902139112088 - Tissue Protector | 2020-04-06 |
| 06902139112125 - Insertion Handle | 2020-04-06 |
| 06902139111579 - Inserter-Extractor for Tibial Nail | 2019-04-23 |
| 06902139111807 - Connecting Screw for Inserter-Extractor | 2019-04-23 |
| 06902139111821 - Connecting Screw, for extracting nails | 2019-04-23 |
| 06902139111890 - Hammer Guide for Slide Hammer | 2019-04-23 |