Primary Device ID | 00889024187047 |
NIH Device Record Key | 347910fb-5241-4e4d-81e3-4a08469a24a1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | 5220-13 |
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@zimmer.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 |
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 | 00889024187047 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-24 |
00889024197992 | 00-5852-054-19 |
00889024197985 | 00-5852-054-18 |
00889024197978 | 00-5852-054-17 |
00889024197961 | 00-5852-054-16 |
00889024197954 | 00-5852-054-15 |
00889024197947 | 00-5852-054-14 |
00889024197930 | 00-5852-054-13 |
00889024197923 | 00-5852-054-12 |
00889024197916 | 00-5852-052-19 |
00889024197909 | 00-5852-052-18 |
00889024197893 | 00-5852-052-17 |
00889024197886 | 00-5852-052-16 |
00889024197879 | 00-5852-052-15 |
00889024197862 | 00-5852-052-14 |
00889024197855 | 00-5852-052-13 |
00889024197848 | 00-5852-052-12 |
00889024197800 | 00-5852-050-19 |
00889024197794 | 00-5852-050-18 |
00889024197787 | 00-5852-050-17 |
00889024197770 | 00-5852-050-16 |
00889024197763 | 00-5852-050-15 |
00889024197756 | 00-5852-050-14 |
00889024197749 | 00-5852-050-13 |
00889024197732 | 00-5852-050-12 |
00889024197695 | 00-5852-042-17 |
00889024197688 | 00-5852-042-09 |
00889024196308 | 00-5850-070-13 |
00889024196292 | 00-5850-070-12 |
00889024196285 | 00-5850-060-26 |
00889024196278 | 00-5850-060-23 |
00889024196261 | 00-5850-060-20 |
00889024196254 | 00-5850-060-17 |
00889024196247 | 00-5850-060-14 |
00889024196230 | 00-5850-060-12 |
00889024196223 | 00-5850-050-26 |
00889024196216 | 00-5850-050-23 |
00889024196209 | 00-5850-050-20 |
00889024196193 | 00-5850-050-17 |
00889024196186 | 00-5850-050-14 |
00889024196179 | 00-5850-050-12 |
00889024196162 | 00-5850-048-20 |
00889024196155 | 00-5850-048-09 |
00889024196148 | 00-5850-048-08 |
00889024196124 | 00-5850-046-45 |
00889024196117 | 00-5850-046-35 |
00889024196100 | 00-5850-046-22 |
00889024196094 | 00-5850-046-20 |
00889024196087 | 00-5850-046-18 |
00889024196070 | 00-5850-046-16 |
00889024196063 | 00-5850-046-14 |