Primary Device ID | 00887868252006 |
NIH Device Record Key | 24a0ce1c-40b6-4f0c-9fe4-ee773811d41f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | JuggerKnot® Soft Anchors |
Version Model Number | 912075 |
Catalog Number | 912075 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | 00887868252006 [Primary] |
MBI | Fastener, fixation, nondegradable, soft tissue |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-05-05 |
Device Publish Date | 2018-09-14 |
00889024664739 - JuggerKnot Short Rigid Reusable Guide | 2024-07-29 |
00889024674288 - HAMMR™ | 2024-07-03 |
00887868555732 - Patient Specific Planning Solution™ | 2024-06-25 |
00880304658462 - Compress® | 2024-05-24 |
00889024663794 - HAMMR™ | 2024-05-17 |
00889024663800 - HAMMR™ | 2024-05-17 |
00889024663817 - HAMMR™ | 2024-05-17 |
00889024663824 - HAMMR™ | 2024-05-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() JUGGERKNOT 97275055 not registered Live/Pending |
Hong, Charles 2022-02-18 |
![]() JUGGERKNOT 86111740 4555637 Live/Registered |
Biomet Sports Medicine, LLC 2013-11-06 |