Primary Device ID | 03599870091272 |
NIH Device Record Key | de760c7e-c085-4a78-b6ec-b96560ee1167 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ENDOBON® |
Version Model Number | ROX20 |
Company DUNS | 186127825 |
Company Name | BIOMET 3I, LLC |
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)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com | |
Phone | +1(800)342-5454 |
3iPBG-CS@biomet.com |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Total Volume | 2 Milliliter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03599870091272 [Primary] |
LYC | Bone grafting material, synthetic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2022-03-10 |
Device Publish Date | 2015-09-10 |
03599870097588 | ENDOBON® XENOGRAFT GRANULES LARGE PARTICLE 8.0ML |
03599870097571 | ENDOBON® XENOGRAFT GRANULES LARGE PARTICLE 5.0ML |
03599870097564 | ENDOBON® XENOGRAFT GRANULES LARGE PARTICLE 2.0ML |
03599870091272 | ENDOBON® XENOGRAFT GRANULES 2.0ML |
03599870091265 | ENDOBON® XENOGRAFT GRANULES 1.0ML |
03599870091258 | ENDOBON® XENOGRAFT GRANULES 0.5ML |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ENDOBON 79077161 3936735 Live/Registered |
BIOMET Deutschland GmbH 2009-04-15 |
ENDOBON 75637719 2403400 Dead/Cancelled |
BIOMET DEUTSCHLAND GMBH 1999-02-10 |