| Primary Device ID | 04046964173295 |
| NIH Device Record Key | 00e23c1a-936a-4fd1-b41c-50a2eac2b3c4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Excia® T |
| Version Model Number | NU218T |
| Catalog Number | NU218T |
| 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 | |
| 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 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 | 04046964173295 [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 |
| 04046964370557 | EXCIA T CEMENTED 12/14 SIZE 20MM |
| 04046964173479 | EXCIA T CEMENTED 12/14 SIZE 14MM |
| 04046964173455 | EXCIA T CEMENTED 12/14 SIZE 10MM |
| 04046964173288 | EXCIA T PLASMAPORE 12/14 SIZE 17MM |
| 04046964173271 | EXCIA T PLASMAPORE 12/14 SIZE 16MM |
| 04046964173264 | EXCIA T PLASMAPORE 12/14 SIZE 15MM |
| 04046964173257 | EXCIA T PLASMAPORE 12/14 SIZE 14MM |
| 04046964173240 | EXCIA T PLASMAPORE 12/14 SIZE 13MM |
| 04046964173233 | EXCIA T PLASMAPORE 12/14 SIZE 12MM |
| 04046964173226 | EXCIA T PLASMAPORE 12/14 SIZE 11MM |
| 04046964173219 | EXCIA T PLASMAPORE 12/14 SIZE 10MM |
| 04046964173202 | EXCIA T PLASMAPORE 12/14 SIZE 9MM |
| 04046964172991 | EXCIA T 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 |