Universal Tibial Nail II, Cannulated 071170255

GUDID 06942782417581

Double Medical Technology Inc.

Tibia nail, non-sterile
Primary Device ID06942782417581
NIH Device Record Key21634ec2-9d3e-43c4-b54b-cfb7293dedcb
Commercial Distribution StatusIn Commercial Distribution
Brand NameUniversal Tibial Nail II, Cannulated
Version Model Number071170255
Catalog Number071170255
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

Length255 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS106942782417581 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HSBRod, Fixation, Intramedullary And Accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[06942782417581]

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 II, Cannulated]

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06942782417710071180345
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06942782417666071180255
06942782417659071170360
06942782417642071170345
06942782417635071170330
06942782417628071170315
06942782417611071170300
06942782417604071170285
06942782417598071170270
06942782417581071170255
06942782417574071160360
06942782417567071160345
06942782417550071160330
06942782417543071160315
06942782417536071160300
06942782417529071160285
06942782417512071160270
06942782417505071160255
06942782416300071180270

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