Primary Device ID | 00887868033001 |
NIH Device Record Key | cf9d9640-fa92-471d-9ff3-8aea3fa6315c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VERSANAIL®TIBIOTALOCALCANEAL (TTC) ANKLE FUSION NAIL |
Version Model Number | 8007-12-030 |
Catalog Number | 800712030 |
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 |
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 |
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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 | 00887868033001 [Primary] |
HRS | PLATE, 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 |
00887868033001 | 8007-12-030 |
00887868032998 | 8007-12-025 |
00887868032981 | 8007-12-020 |
00887868032974 | 8007-12-015 |
00887868032967 | 8007-10-030 |
00887868032950 | 8007-10-025 |
00887868032943 | 8007-10-020 |
00887868032936 | 8007-10-015 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VERSANAIL 78080212 2728157 Live/Registered |
BIOMET C.V. 2001-08-20 |