Primary Device ID | 06942782450267 |
NIH Device Record Key | fd60ac32-2ca3-4c65-b0f1-c47911250f07 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Clavicular Locking Plate |
Version Model Number | 020032011 |
Catalog Number | 020032011 |
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 | |
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 | |
Phone | +865926087101 |
info@double-medical.com | |
Phone | +865926087101 |
info@double-medical.com | |
Phone | +865926087101 |
info@double-medical.com |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Millimeter |
Width | 10 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06942782450267 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
Moist Heat or Steam Sterilization
[06942782450267]
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 |
06942782450274 | 020032012 |
06942782450267 | 020032011 |
06942782450250 | 020032010 |
06942782450243 | 020031012 |
06942782450236 | 020031011 |
06942782450229 | 020031010 |
06942782407520 | 020032009 |
06942782407513 | 020032008 |
06942782407506 | 020032007 |
06942782407490 | 020032006 |
06942782407483 | 020032005 |
06942782407476 | 020032004 |
06942782407469 | 020031009 |
06942782407452 | 020031008 |
06942782407445 | 020031007 |
06942782407438 | 020031006 |
06942782407421 | 020031005 |
06942782407414 | 020031004 |