| Primary Device ID | 06942782475260 |
| NIH Device Record Key | 291390cc-c47e-4f5c-a156-ad094de9d1e5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Proximal Femoral Locking Plate II |
| Version Model Number | 020972000 |
| Catalog Number | 020972000 |
| 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 | 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 |
| Phone | +865926087101 |
| info@double-medical.com | |
| Phone | +865926087101 |
| info@double-medical.com |
| Device Size Text, specify | 0 |
| Length | 43 Millimeter |
| Width | 14.12 Millimeter |
| Device Size Text, specify | 0 |
| Length | 43 Millimeter |
| Width | 14.12 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06942782475260 [Primary] |
| HWC | Screw, Fixation, Bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[06942782475260]
Moist Heat or Steam Sterilization
[06942782475260]
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 |
| 06942782475260 | 020972000 |
| 06942782475253 | 020971000 |