TDT2.8L10

GUDID 03700569605520

NEWCLIP TECHNICS

Orthopaedic bone screw, non-bioabsorbable, non-sterile
Primary Device ID03700569605520
NIH Device Record Key115ef201-c163-4b53-9c2d-ae5e5b15146d
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberTDT2.8L10
Catalog NumberTDT2.8L10
Company DUNS263281904
Company NameNEWCLIP TECHNICS
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS103700569605520 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, Fixation, Bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03700569605520]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-02-19
Device Publish Date2017-03-14

Devices Manufactured by NEWCLIP TECHNICS

03700569602475 - Activmotion2024-11-21
03700569602499 - Activmotion2024-11-21
03700569607586 - Alians Clavicle2024-11-21
03700569607609 - Alians Clavicle2024-11-21
03700569608958 - Alians Clavicle2024-11-21
03700569608972 - Alians Clavicle2024-11-21
03700569608989 - Alians Clavicle2024-11-21
03700569608996 - Alians Clavicle2024-11-21

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.