Primary Device ID | 00880304482067 |
NIH Device Record Key | b9d0e49b-3311-4049-ae4c-58f2c6a7fa2b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VANGUARD SSK360/DA360 KNEE SYSTEM |
Version Model Number | 185286 |
Catalog Number | 185286 |
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 | 00880304482067 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-12-11 |
Device Publish Date | 2015-10-24 |
00880304482128 | 185287 |
00880304482111 | 185285 |
00880304482104 | 185283 |
00880304482098 | 185281 |
00880304482081 | 185290 |
00880304482074 | 185288 |
00880304482067 | 185286 |
00880304482050 | 185284 |
00880304482043 | 185282 |
00880304482036 | 185280 |
00880304482029 | 185267 |
00880304482012 | 185265 |
00880304482005 | 185263 |
00880304481992 | 185261 |
00880304481985 | 185270 |
00880304481978 | 185268 |
00880304481961 | 185266 |
00880304481954 | 185264 |
00880304481947 | 185262 |
00880304467422 | 185260 |