Zimmer Biomet® Freedom® Head 110040313
GUDID 00889024625839
Zimmer, Inc.
Instrument tray, reusable| Primary Device ID | 00889024625839 |
| NIH Device Record Key | 86890a35-80d5-4746-ad6b-4e8cf424618e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Zimmer Biomet® Freedom® Head |
| Version Model Number | 110040313 |
| Catalog Number | 110040313 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| 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 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024625839 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K183457
FDA Product Code
| KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
[00889024625839]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-15 |
| Device Publish Date | 2024-11-07 |
Devices Manufactured by Zimmer, Inc.
| 00889024685581 - MODIFIED EXACT OFFSET BROACH HANDLE | 2025-03-11 |
| 00889024687288 - Reusable 3.2mm Pin - 178mm long | 2025-03-11 |
| 00889024687431 - SPRING PLUNGER ASSY, STD | 2025-03-11 |
| 00889024687448 - SPRING PLUNGER ASSY, AGGRESSIVE | 2025-03-11 |
| 00889024658134 - Persona® Knee System | 2025-02-14 |
| 00889024658141 - Persona® Knee System | 2025-02-14 |
| 00889024658158 - Persona® Knee System | 2025-02-14 |
| 00889024658165 - Persona® Knee System | 2025-02-14 |
Trademark Results [Zimmer Biomet]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ZIMMER BIOMET 88381597 5913232 Live/Registered |
Zimmer, Inc. 2019-04-11 |
 ZIMMER BIOMET 86880421 5880337 Live/Registered |
Zimmer, Inc. 2016-01-20 |
 ZIMMER BIOMET 86692147 not registered Dead/Abandoned |
Zimmer Biomet Holdings, Inc. 2015-07-14 |
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