Primary Device ID | 00889024583535 |
NIH Device Record Key | d8a06d81-dc7b-4373-b4d2-125180e72abf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Narrow Persona P-Ref 4-in-1 Cut Guide |
Version Model Number | SSI005435 |
Catalog Number | SSI005435 |
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 | 00889024583535 [Primary] |
JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
Moist Heat or Steam Sterilization
[00889024583535]
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 |