Excia® L NK605T

GUDID 04046963089696

EXCIA L PLASMAPORE 12/14 SIZE 15MM

Aesculap AG

Coated hip femur prosthesis, modular
Primary Device ID04046963089696
NIH Device Record Keyefce7c09-c5ad-4396-bdf1-c0b4a392db10
Commercial Distribution StatusIn Commercial Distribution
Brand NameExcia® L
Version Model NumberNK605T
Catalog NumberNK605T
Company DUNS315018218
Company NameAesculap AG
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

Customer Support Contacts

Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(800)282-9000
EmailGUDID.BBMUS_Service@bbraun.com
Phone+1(800)282-9000
EmailGUDID.BBMUS_Service@bbraun.com
Phone+1(800)282-9000
EmailGUDID.BBMUS_Service@bbraun.com
Phone+1(800)282-9000
EmailGUDID.BBMUS_Service@bbraun.com
Phone+1(800)282-9000
EmailGUDID.BBMUS_Service@bbraun.com
Phone+1(800)282-9000
EmailGUDID.BBMUS_Service@bbraun.com
Phone+1(800)282-9000
EmailGUDID.BBMUS_Service@bbraun.com
Phone+1(800)282-9000
EmailGUDID.BBMUS_Service@bbraun.com
Phone+1(800)282-9000
EmailGUDID.BBMUS_Service@bbraun.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104046963089696 [Primary]

FDA Product Code

LZOProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-11-20
Device Publish Date2015-09-24

On-Brand Devices [Excia® L]

04046963089894EXCIA L CEMENTED 12/14 SIZE 18MM
04046963089887EXCIA L CEMENTED 12/14 SIZE 17MM
04046963089870EXCIA L CEMENTED 12/14 SIZE 16MM
04046963089863EXCIA L CEMENTED 12/14 SIZE 15MM
04046963089856EXCIA L CEMENTED 12/14 SIZE 14MM
04046963089832EXCIA L CEMENTED 12/14 SIZE 12MM
04046963089825EXCIA L CEMENTED 12/14 SIZE 11MM
04046963089818EXCIA L CEMENTED 12/14 SIZE 10MM
04038653462551EXCIA L PLASMAPORE-µCAP 8/10 SIZE 18MM
04038653462544EXCIA L PLASMAPORE-µCAP 8/10 SIZE 17MM
04038653462537EXCIA L PLASMAPORE-µCAP 8/10 SIZE 16MM
04038653462520EXCIA L PLASMAPORE-µCAP 8/10 SIZE 15MM
04038653462513EXCIA L PLASMAPORE-µCAP 8/10 SIZE 14MM
04038653462506EXCIA L PLASMAPORE-µCAP 8/10 SIZE 13MM
04038653462490EXCIA L PLASMAPORE-µCAP 8/10 SIZE 12MM
04038653462483EXCIA L PLASMAPORE-µCAP 8/10 SIZE 11MM
04038653462476EXCIA L PLASMAPORE-µCAP 8/10 SIZE 10MM
04038653462469EXCIA L PLASMAPORE-µCAP 8/10 SIZE 9MM
04038653462452EXCIA L PLASMAPORE-µCAP 8/10 SIZE 8MM
04046963089849EXCIA L CEMENTED 12/14 SIZE 13MM
04046963089696EXCIA L PLASMAPORE 12/14 SIZE 15MM
04046963089658EXCIA L PLASMAPORE 12/14 SIZE 11MM
04046963089627EXCIA L PLASMAPORE 12/14 SIZE 8MM

Trademark Results [Excia]

Mark Image

Registration | Serial
Company
Trademark
Application Date
EXCIA
EXCIA
87525875 not registered Live/Pending
ALBION CO., LTD.
2017-07-12
EXCIA
EXCIA
78533538 3110488 Live/Registered
AESCULAP IMPLANT SYSTEMS, LLC
2004-12-16
EXCIA
EXCIA
76626739 3099785 Live/Registered
AESCULAP AG
2005-01-03
EXCIA
EXCIA
76548499 not registered Dead/Abandoned
Albion Cosmetics Co., Ltd.
2003-10-02

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