Selex® S063136
GUDID 00887868512162
Biomet Orthopedics, LLC
Femoral head prosthesis trial| Primary Device ID | 00887868512162 |
| NIH Device Record Key | 56111abd-4e46-4e15-b743-4a5c956f41a5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Selex® |
| Version Model Number | S063136 |
| Catalog Number | S063136 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 | false |
| 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 |
Customer Support Contacts
Device Dimensions
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868512162 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K062997
FDA Product Code
| HWT | TEMPLATE |
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
[00887868512162]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-05-16 |
| Device Publish Date | 2022-05-08 |
On-Brand Devices [Selex®]
| 00887868512186 | S313131 |
| 00887868411168 | S333136 |
| 00887868512193 | S313132 |
| 00887868512308 | S993136 |
| 00887868512292 | S663136 |
| 00887868512179 | S123136 |
| 00887868512162 | S063136 |
| 00887868512155 | S033136 |
| 00887868512148 | S003136 |
Trademark Results [Selex]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SELEX 90534496 not registered Live/Pending |
APTAMIN LAB CO., LTD. 2021-02-18 |
 SELEX 90402076 not registered Live/Pending |
MAEIL DAIRIES CO., LTD. 2020-12-22 |
 SELEX 90402011 not registered Live/Pending |
MAEIL DAIRIES CO., LTD. 2020-12-22 |
 SELEX 81040054 1040054 Dead/Cancelled |
Picollo; Giacomo 0000-00-00 |
 SELEX 81019184 1019184 Dead/Cancelled |
National Chemsearch Corporation 0000-00-00 |
 SELEX 79033619 3612515 Live/Registered |
LEONARDO S.p.A. 2005-10-05 |
 SELEX 79029965 3237728 Dead/Cancelled |
ADAPTIVE PLASMA TECHNOLOGY; CORPORATION 2005-10-13 |
 SELEX 78958031 3256369 Dead/Cancelled |
Selex Footwear, Inc. 2006-08-22 |
 SELEX 78148410 2929597 Live/Registered |
Biomet Manufacturing, LLC 2002-07-29 |
 SELEX 77745926 3861697 Dead/Cancelled |
Money Store, LP, The 2009-05-27 |
 SELEX 77745919 3861696 Dead/Cancelled |
The Money Store, LP 2009-05-27 |
 SELEX 76534082 not registered Dead/Abandoned |
PALLADIO TRADING, INC. 2003-07-31 |
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