| Primary Device ID | 07613327123753 |
| NIH Device Record Key | 7ecdcc2b-f757-4c97-838b-e5d87df58926 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EXETER |
| Version Model Number | 0580-3-321 |
| Catalog Number | 0580-3-321 |
| Company DUNS | 058311945 |
| Company Name | Howmedica Osteonics Corp. |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 205 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327123753 [Primary] |
| KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2018-05-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() EXETER 90559649 not registered Live/Pending |
EQT AB 2021-03-04 |
![]() EXETER 87768494 not registered Live/Pending |
Exeter Finance LLC 2018-01-24 |
![]() EXETER 87131287 not registered Dead/Abandoned |
Reed, David 2016-08-08 |
![]() EXETER 86652227 5402003 Live/Registered |
DataPoint International, LLC 2015-06-04 |
![]() EXETER 85911192 4610653 Live/Registered |
DST Health Solutions, LLC 2013-04-22 |
![]() EXETER 85708626 4621652 Live/Registered |
DST Health Solutions, LLC 2012-08-21 |
![]() EXETER 85612906 4877845 Dead/Cancelled |
Exeter Finance Corp. 2012-05-01 |
![]() EXETER 81038864 1038864 Dead/Cancelled |
Scott & Fetzer Company, The 0000-00-00 |
![]() EXETER 78070778 2765618 Live/Registered |
XCaliber International Ltd., L.L.C. 2001-06-25 |
![]() EXETER 77779827 3728400 Live/Registered |
Pyramex Safety Products, LLC 2009-07-13 |
![]() EXETER 77250908 3702155 Dead/Cancelled |
BULOVA CORPORATION 2007-08-09 |
![]() EXETER 76654364 not registered Dead/Abandoned |
Strathmore Partners LP 2006-01-27 |