Fitmore® Hip Stem 01.00555.102
GUDID 00889024655836
Zimmer GmbH
Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable| Primary Device ID | 00889024655836 |
| NIH Device Record Key | b07ccc3f-7519-4920-88b1-719ae68620bd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fitmore® Hip Stem |
| Version Model Number | 01.00555.102 |
| Catalog Number | 01.00555.102 |
| Company DUNS | 488133448 |
| Company Name | Zimmer GmbH |
| 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 | true |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024655836 [Primary] |
FDA Product Code
| KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
[00889024655836]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-03-03 |
| Device Publish Date | 2023-02-23 |
On-Brand Devices [Fitmore® Hip Stem]
Trademark Results [Fitmore]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FITMORE 97066514 not registered Live/Pending |
Shenzhen Wanlisheng technology co., ltd 2021-10-08 |
 FITMORE 97007162 not registered Live/Pending |
Chengdu Yaoyao Erba Technology Co., Ltd. 2021-09-01 |
 FITMORE 77265360 3506235 Live/Registered |
Zimmer GmbH 2007-08-27 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.