Primary Device ID | 00887868343612 |
NIH Device Record Key | e0c02ce1-b87a-4abd-aca7-b44f034b8381 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Prelude® PF |
Version Model Number | 110005118 |
Catalog Number | 110005118 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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)348-9500 |
customerservice@zimmerbiomet.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868343612 [Primary] |
KRR | PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-10-21 |
Device Publish Date | 2019-10-11 |
00887868343735 | 110018164 |
00887868343728 | 110018156 |
00887868343711 | 110018155 |
00887868343704 | 110018154 |
00887868343698 | 110018153 |
00887868343681 | 110018152 |
00887868343674 | 110018151 |
00887868343667 | 110018150 |
00887868343650 | 110018149 |
00887868343643 | 110018148 |
00887868343636 | 110005120 |
00887868343629 | 110005119 |
00887868343612 | 110005118 |
00887868343605 | 110005117 |
00887868343599 | 110005116 |
00887868343582 | 110005115 |
00887868343575 | 110004335 |
00887868343568 | 110004334 |
00887868343551 | 110004333 |
00887868343544 | 110004332 |
00887868343537 | 110004331 |
00887868343520 | 110004330 |
Mark Image Registration | Serial | Company Trademark Application Date |
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