Universal Tibial Nail, Solid 070050360

GUDID 06902139071521

Double Medical Technology Inc.

Tibia nail, non-sterile
Primary Device ID06902139071521
NIH Device Record Keya12ebfde-35fd-46c1-b58a-5a0f3afa3ef5
Commercial Distribution StatusIn Commercial Distribution
Brand NameUniversal Tibial Nail, Solid
Version Model Number070050360
Catalog Number070050360
Company DUNS529366055
Company NameDouble Medical Technology Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+865926087101
Emailinfo@double-medical.com

Device Dimensions

Length360 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS106902139071521 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HSBRod, Fixation, Intramedullary And Accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[06902139071521]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-01

On-Brand Devices [Universal Tibial Nail, Solid]

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06942782486501070060285
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06942782457082070040360
06942782414368070040345
06942782413439070050345
06942782413422070050330
06942782413415070050315
06942782413408070050300
06942782413392070050285
06942782413385070050270
06942782413378070040330
06942782413361070040315
06942782413354070040300
06942782413347070040285
06942782413330070040270
06902139071538070060360
06902139071521070050360

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