Primary Device ID | 00885556143131 |
NIH Device Record Key | 33630da6-bdf6-41ea-9ea9-7f271493e290 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | META |
Version Model Number | 71934244 |
Catalog Number | 71934244 |
Company DUNS | 109903521 |
Company Name | Smith & Nephew, Inc. |
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)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00885556143131 [Primary] |
JDS | NAIL, 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 | 2015-08-29 |
00885556143148 | TRIGEN META RETRO FEMORAL NAIL 10MM X 38CM W/ML HOLE |
00885556143131 | TRIGEN META RETRO FEMORAL NAIL 10MM X 40CM W/ML HOLE |
00885556143124 | TRIGEN META RETRO FEMORAL NAIL 13MM X 36CM W/ML HOLE |
00885556068007 | TRIGEN META RETRO FEMORAL NAIL 13MM X 40CM W/ML HOLE |
00885556067482 | TRIGEN META RETRO FEMORAL NAIL 13MM X 38CM W/ML HOLE |
00885556066881 | TRIGEN META RETRO FEMORAL NAIL 10MM X 36CM W/ML HOLE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
META 98713780 not registered Live/Pending |
Meta-Regalbau GmbH & Co. Kommanditgesellschaft 2024-08-23 |
META 98539974 not registered Live/Pending |
Metabev IP Holdings LLC 2024-05-08 |
META 98203349 not registered Live/Pending |
Schmidt & Bender GmbH & Co. KG 2023-09-29 |
META 97979391 not registered Live/Pending |
Meta Platforms, Inc. 2022-01-04 |
META 97979116 not registered Live/Pending |
Meta Platforms, Inc. 2022-01-04 |
META 97979027 not registered Live/Pending |
Meta Platforms, Inc. 2022-01-04 |
META 97978832 not registered Live/Pending |
Meta Platforms, Inc. 2022-01-04 |
META 97978476 not registered Live/Pending |
Meta Platforms, Inc. 2022-01-04 |
META 97744546 not registered Live/Pending |
Metabev LLC 2023-01-06 |
META 97653284 not registered Live/Pending |
Metabev LLC 2022-10-28 |
META 97605021 not registered Live/Pending |
Metabev LLC 2022-09-23 |
META 97600584 not registered Live/Pending |
Metabev LLC 2022-09-21 |