Primary Device ID | 04046964173318 |
NIH Device Record Key | ccf3c466-3192-4095-a921-8128f7033776 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Excia® T |
Version Model Number | NU220T |
Catalog Number | NU220T |
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(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.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 Issuing Agency | Device ID |
---|---|
GS1 | 04046964173318 [Primary] |
LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2024-11-20 |
Device Publish Date | 2015-11-11 |
04046964173493 | EXCIA T CEMENTED 12/14 SIZE 18MM |
04046964173486 | EXCIA T CEMENTED 12/14 SIZE 16MM |
04046964173462 | EXCIA T CEMENTED 12/14 SIZE 12MM |
04046964173318 | EXCIA T PLASMAPORE 12/14 SIZE 20MM |
04046964173301 | EXCIA T PLASMAPORE 12/14 SIZE 19MM |
04046964173295 | EXCIA T PLASMAPORE 12/14 SIZE 18MM |
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 |