Primary Device ID | 06942782452506 |
NIH Device Record Key | dc12239a-a879-455e-9165-bb1c2e9323e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Proximal Humeral Locking Plate Ⅱ, Combi-holes |
Version Model Number | 020380005 |
Catalog Number | 020380005 |
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 |
Width | 12 Millimeter |
Length | 123.1 Millimeter |
Device Size Text, specify | 0 |
Width | 12 Millimeter |
Length | 123.1 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06942782452506 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[06942782452506]
Moist Heat or Steam Sterilization
[06942782452506]
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 |
06942782452582 | 020380013 |
06942782452575 | 020380012 |
06942782452568 | 020380011 |
06942782452551 | 020380010 |
06942782452544 | 020380009 |
06942782452537 | 020380008 |
06942782452520 | 020380007 |
06942782452513 | 020380006 |
06942782452506 | 020380005 |
06942782452490 | 020380004 |
06942782452483 | 020380003 |