Primary Device ID | 04046963089894 |
NIH Device Record Key | 9753275b-fd74-4557-80ac-0d0cf10cf617 |
Commercial Distribution Discontinuation | 2018-11-04 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Excia® L |
Version Model Number | NK998K |
Catalog Number | NK998K |
Company DUNS | 315018218 |
Company Name | Aesculap AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04046963089894 [Primary] |
JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2021-04-23 |
Device Publish Date | 2015-09-24 |
04046963089894 | EXCIA L CEMENTED 12/14 SIZE 18MM |
04046963089887 | EXCIA L CEMENTED 12/14 SIZE 17MM |
04046963089870 | EXCIA L CEMENTED 12/14 SIZE 16MM |
04046963089863 | EXCIA L CEMENTED 12/14 SIZE 15MM |
04046963089856 | EXCIA L CEMENTED 12/14 SIZE 14MM |
04046963089832 | EXCIA L CEMENTED 12/14 SIZE 12MM |
04046963089825 | EXCIA L CEMENTED 12/14 SIZE 11MM |
04046963089818 | EXCIA L CEMENTED 12/14 SIZE 10MM |
04038653462551 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 18MM |
04038653462544 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 17MM |
04038653462537 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 16MM |
04038653462520 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 15MM |
04038653462513 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 14MM |
04038653462506 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 13MM |
04038653462490 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 12MM |
04038653462483 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 11MM |
04038653462476 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 10MM |
04038653462469 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 9MM |
04038653462452 | EXCIA L PLASMAPORE-µCAP 8/10 SIZE 8MM |
04046963089849 | EXCIA L CEMENTED 12/14 SIZE 13MM |
04046963089696 | EXCIA L PLASMAPORE 12/14 SIZE 15MM |
04046963089658 | EXCIA L PLASMAPORE 12/14 SIZE 11MM |
04046963089627 | EXCIA L PLASMAPORE 12/14 SIZE 8MM |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EXCIA 87525875 not registered Live/Pending |
ALBION CO., LTD. 2017-07-12 |
EXCIA 78533538 3110488 Live/Registered |
AESCULAP IMPLANT SYSTEMS, LLC 2004-12-16 |
EXCIA 76626739 3099785 Live/Registered |
AESCULAP AG 2005-01-03 |
EXCIA 76548499 not registered Dead/Abandoned |
Albion Cosmetics Co., Ltd. 2003-10-02 |