Phoenix™ Retrograde Femoral Nail Instruments 14-444001
GUDID 00887868560859
Biomet Orthopedics, LLC
Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable| Primary Device ID | 00887868560859 |
| NIH Device Record Key | 42b4a7eb-07df-4403-bb8d-4fbf5458c949 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Phoenix™ Retrograde Femoral Nail Instruments |
| Version Model Number | 14-444001 |
| Catalog Number | 14-444001 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868560859 [Primary] |
FDA Product Code
| FSM | TRAY, SURGICAL, INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
[00887868560859]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-15 |
| Device Publish Date | 2023-09-07 |
Devices Manufactured by Biomet Orthopedics, LLC
| 00887868004087 - PRIMARY TREPHINE | 2024-04-03 |
| 00887868004094 - BUSHING | 2024-04-03 |
| 00887868004100 - SECONDARY TREPHINE | 2024-04-03 |
| 00887868048272 - TREPHINE | 2024-04-03 |
| 00887868048289 - TREPHINE | 2024-04-03 |
| 00887868048296 - TREPHINE | 2024-04-03 |
| 00887868048302 - TREPHINE | 2024-04-03 |
| 00880304658387 - Compress® | 2024-03-11 |
Trademark Results [Phoenix]
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