Primary Device ID | 00887868057557 |
NIH Device Record Key | 105f2c93-b017-4d23-8fa9-5b4554418e3e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FRS™CANNULATED SCREW |
Version Model Number | 8520-25-014 |
Catalog Number | 852025014 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, 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)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868057557 [Primary] |
HWC | Screw, fixation, bone |
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 | 2015-10-24 |
00887868057724 | 8520-30-034 |
00887868057717 | 8520-30-032 |
00887868057700 | 8520-30-030 |
00887868057694 | 8520-30-028 |
00887868057687 | 8520-30-026 |
00887868057670 | 8520-30-024 |
00887868057663 | 8520-30-022 |
00887868057656 | 8520-30-020 |
00887868057649 | 8520-30-018 |
00887868057632 | 8520-30-016 |
00887868057625 | 8520-30-014 |
00887868057618 | 8520-25-026 |
00887868057601 | 8520-25-024 |
00887868057595 | 8520-25-022 |
00887868057588 | 8520-25-020 |
00887868057571 | 8520-25-018 |
00887868057564 | 8520-25-016 |
00887868057557 | 8520-25-014 |
00887868057540 | 8520-25-012 |
00887868057533 | 8520-25-010 |