Persona® 42-5830-055-00
GUDID 00889024563131
Zimmer, Inc.
Surgical torque wrench, reusable| Primary Device ID | 00889024563131 |
| NIH Device Record Key | 4a9b8f79-8033-4203-94f7-e282c4c4da38 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Persona® |
| Version Model Number | 42-5830-055-00 |
| Catalog Number | 42-5830-055-00 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| 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
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024563131 [Primary] |
FDA Product Code
| HXC | WRENCH |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024563131]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-18 |
| Device Publish Date | 2019-04-10 |
On-Brand Devices [Persona®]
Trademark Results [Persona]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.