Primary Device ID | 00889024044524 |
NIH Device Record Key | 3598a3bf-5166-4fee-ba57-f7ee5fd42979 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | M/DN® |
Version Model Number | 2253-320-08 |
Catalog Number | 00-2253-320-08 |
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 | true |
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 |
Device Size Text, specify | 0 |
Length | 32 Centimeter |
Device Size Text, specify | 0 |
Length | 32 Centimeter |
Device Size Text, specify | 0 |
Length | 32 Centimeter |
Device Size Text, specify | 0 |
Length | 32 Centimeter |
Device Size Text, specify | 0 |
Length | 32 Centimeter |
Device Size Text, specify | 0 |
Length | 32 Centimeter |
Device Size Text, specify | 0 |
Length | 32 Centimeter |
Device Size Text, specify | 0 |
Length | 32 Centimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024044524 [Primary] |
HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-09-13 |
Device Publish Date | 2015-09-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() M/DN 75241965 2166590 Live/Registered |
ZIMMER, INC 1997-02-14 |