Primary Device ID | 00889024563193 |
NIH Device Record Key | 9543c9fb-3ffc-44d3-a1b7-1127fd2b6276 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Persona® |
Version Model Number | 00-5901-035-48 |
Catalog Number | 00-5901-035-48 |
Company DUNS | 056038268 |
Company Name | Zimmer, Inc. |
Device Count | 2 |
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 | true |
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)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Size Text, specify | 0 |
Length | 48 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024563193 [Primary] |
GS1 | 70889024563192 [Unit of Use] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-07-12 |
Device Publish Date | 2019-04-10 |