Arsenal Ankle Forceps

GUDID 00810028391895

Trilliant Surgical, LLC

Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers Bone fixation plate pliers
Primary Device ID00810028391895
NIH Device Record Key3f1120b8-62c2-4538-ab66-bf212f097531
Commercial Distribution StatusIn Commercial Distribution
Brand NameArsenal Ankle Forceps
Version Model Number340-00-019
Company DUNS828829072
Company NameTrilliant Surgical, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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
GS100810028391895 [Primary]

FDA Product Code

HTDForceps

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


[00810028391895]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-10
Device Publish Date2022-05-02

Devices Manufactured by Trilliant Surgical, LLC

00810028395343 - Revision MTP Plate, L, 0°2024-04-04
00810028394995 - Cannulated Depth Gauge2024-03-29
00810028395022 - 2.0/2.4 Cannulated Driver Bit 2024-03-29
00810028395039 - 3.0/4.0 Cannulated Driver2024-03-29
00810028395046 - 2.0/2.4 Removal Tool2024-03-29
00810028395053 - 3.0/4.0 Removal Bit2024-03-29
00810028395060 - Screw Removal Tool2024-03-29
00810028395145 - 5" K-Wire Tube, Double Ended2024-03-29

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