Aria Trial Neck

GUDID 09348215040369

SIGNATURE ORTHOPAEDICS PTY LTD

Surgical implant template, reusable
Primary Device ID09348215040369
NIH Device Record Key3cec11d0-c7fd-47d2-98ee-4792d947126a
Commercial Distribution StatusIn Commercial Distribution
Brand NameAria Trial Neck
Version Model Number111-20-6254
Company DUNS751993028
Company NameSIGNATURE ORTHOPAEDICS PTY LTD
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS109348215040369 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
LXHOrthopedic Manual Surgical Instrument
MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


[09348215040369]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-06-18
Device Publish Date2018-10-02

On-Brand Devices [Aria Trial Neck]

09348215040413111-20-6264
09348215040406111-20-6263
09348215040390111-20-6262
09348215040383111-20-6261
09348215040376111-20-6260
09348215040369111-20-6254
09348215040352111-20-6253
09348215040345111-20-6252
09348215040338111-20-6251
09348215040321111-20-6250

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