Primary Device ID | 00889024013315 |
NIH Device Record Key | 4ef58f61-2d61-42a4-b8d7-90f11994a6c8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Spline® Twist™ Implant System |
Version Model Number | 2135 |
Company DUNS | 103167086 |
Company Name | ZIMMER DENTAL INC. |
Device Count | 1 |
DM Exempt | true |
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 |
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 |
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 |
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 |
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 | 00889024013315 [Primary] |
DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
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 | 2015-10-21 |
00889024013315 | 2135 |
00889024013308 | 2133 |
00889024013292 | 2131 |
00889024013285 | 2130 |
00889024013278 | 2121 |
00889024013261 | 2120 |
00889024013193 | 1996 |
00889024013186 | 1995 |
00889024013179 | 1994 |
00889024013162 | 1993 |
00889024013155 | 1992 |
00889024013148 | 1991 |
00889024013131 | 1990 |
00889024013124 | 1989 |
00889024013117 | 1988 |
00889024013100 | 1987 |
00889024013094 | 1986 |
00889024013087 | 1985 |
00889024013070 | 1984 |
00889024013063 | 1983 |
00889024013056 | 1982 |
00889024013049 | 1981 |
00889024013032 | 1980 |
00889024013025 | 1979 |
00889024013018 | 1961 |
00889024013001 | 1960 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SPLINE 86812634 5152234 Live/Registered |
KAI U.S.A., Ltd. 2015-11-06 |
SPLINE 86093919 4898978 Live/Registered |
ARISTA NETWORKS, INC. 2013-10-17 |
SPLINE 79355710 not registered Live/Pending |
DT Swiss Deutschland GmbH 2022-08-23 |
SPLINE 79114485 4359585 Live/Registered |
DT Swiss AG 2012-05-21 |
SPLINE 75475816 2271901 Live/Registered |
ZIMMER DENTAL INC. 1998-04-28 |
SPLINE 74615238 2099807 Dead/Cancelled |
MITSUBISHI ELECTRIC INFORMATION TECHNOLOGY CENTER AMERICA INC. 1994-12-27 |