Primary Device ID | 06942782405618 |
NIH Device Record Key | 39e6cf16-d86a-4217-970f-1346a6487fb9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Distal Fibular Locking Plate |
Version Model Number | 020202002 |
Catalog Number | 020202002 |
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 | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Size Text, specify | 0 |
Length | 66.5 Millimeter |
Width | 10.4 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06942782405618 [Primary] |
HRS | Plate, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
Moist Heat or Steam Sterilization
[06942782405618]
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 |
06942782417888 | 020202010 |
06942782417871 | 020201010 |
06942782407964 | 020202009 |
06942782407957 | 020201009 |
06942782405618 | 020202002 |
06942782405601 | 020201002 |
06942782405021 | 020202008 |
06942782405014 | 020202007 |
06942782405007 | 020202006 |
06942782404994 | 020202005 |
06942782404987 | 020202004 |
06942782404970 | 020202003 |
06942782404963 | 020201008 |
06942782404956 | 020201007 |
06942782404949 | 020201006 |
06942782404932 | 020201005 |
06942782404925 | 020201004 |
06942782404918 | 020201003 |