ARCADIUS MC914R

GUDID 04046955088485

ARCADIUS DISTRACTOR INSERTER SPLIT PIN

AESCULAP IMPLANT SYSTEMS, LLC

Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable
Primary Device ID04046955088485
NIH Device Record Key7cbf0948-ac03-4c6b-a010-760c116ce7fa
Commercial Distribution StatusIn Commercial Distribution
Brand NameARCADIUS
Version Model NumberMC914R
Catalog NumberMC914R
Company DUNS622600992
Company NameAESCULAP IMPLANT SYSTEMS, 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

Customer Support Contacts

Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104046955088485 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


[04046955088485]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-09
Device Publish Date2020-10-30

On-Brand Devices [ARCADIUS]

04046955091102ARCADIUS PUSHING BLOCK 14/6
04046955091096ARCADIUS PUSHING BLOCK 12/6
04046955091089ARCADIUS PUSHING BLOCK 10/6
04046955091072ARCADIUS PUSHING BLOCK 20/3
04046955091065ARCADIUS PUSHING BLOCK 18/3
04046955091058ARCADIUS PUSHING BLOCK 16/3
04046955091041ARCADIUS PUSHING BLOCK 14/3
04046955088652ARCADIUS XP L DISTRACTOR INSERTER
04046955088645ARCADIUS PUSHING BLOCK 20/6
04046955088638ARCADIUS PUSHING BLOCK 18/6
04046955088621ARCADIUS PUSHING BLOCK 16/6
04046955088614ARCADIUS PUSHING BLOCK 12/3
04046955088607ARCADIUS PUSHING BLOCK 10/3
04046955088485ARCADIUS DISTRACTOR INSERTER SPLIT PIN

Trademark Results [ARCADIUS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ARCADIUS
ARCADIUS
85873454 4418397 Live/Registered
Aesculap Implant Systems, LLC
2013-03-12
ARCADIUS
ARCADIUS
78672233 3157204 Dead/Cancelled
Arcadia Group North Carolina, LLC
2005-07-18

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