| Primary Device ID | 00889024583474 |
| NIH Device Record Key | 7eb2353f-828c-4948-889a-2ea4ddb2a53e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Narrow Persona P-Ref 4-in-1 Cut Guide |
| Version Model Number | SSI005429 |
| Catalog Number | SSI005429 |
| 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 | false |
| Serial Number | true |
| 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 |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024583474 [Primary] |
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
[00889024583474]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-02-19 |
| Device Publish Date | 2020-02-11 |
| 00889024583535 | SSI005435 |
| 00889024583528 | SSI005434 |
| 00889024583511 | SSI005433 |
| 00889024583504 | SSI005432 |
| 00889024583498 | SSI005431 |
| 00889024583481 | SSI005430 |
| 00889024583474 | SSI005429 |
| 00889024583467 | SSI005428 |
| 00889024583450 | SSI005427 |
| 00889024583443 | SSI005426 |