Primary Device ID | 06942782452148 |
NIH Device Record Key | 9e93aba2-2aea-4aaf-ade1-8c3814a4ae03 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Proximal Lateral Tibial Locking Plate |
Version Model Number | 020712013 |
Catalog Number | 020712013 |
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 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Width | 10 Millimeter |
Length | 180.85 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06942782452148 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
Moist Heat or Steam Sterilization
[06942782452148]
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 |
06942782452155 | 020712017 |
06942782452148 | 020712013 |
06942782452131 | 020712009 |
06942782452124 | 020712005 |
06942782452117 | 020711017 |
06942782452100 | 020711013 |
06942782452094 | 020711009 |
06942782452087 | 020711005 |