Primary Device ID | 00887482151976 |
NIH Device Record Key | 61da730c-82ee-453e-bccd-a91049e4e67e |
Commercial Distribution Discontinuation | 9999-01-01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Olsen® |
Version Model Number | 90-9522-S |
Catalog Number | 90-9522-S |
Company DUNS | 079641356 |
Company Name | SYMMETRY SURGICAL INC. |
Device Count | 10 |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Special Storage Condition, Specify | Between 0 and 0 *Store in Dry, clean and safe place |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887482122119 [Unit of Use] |
GS1 | 00887482151976 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
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 | 2016-12-14 |
00887482151976 | L Hook Laparoscopic Electrode, Single Use, Sterile, Length 13 Inches |
00887482151969 | Spatula Laparoscopic Electrode, 33CM Sterile, Single Use |
00887482151952 | J-Hook Laparoscopic Electrode, 33CM, Sterile Single Use |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OLSEN 88894439 not registered Live/Pending |
CESAR AUGUSTO OLSEN 2020-04-30 |
OLSEN 88638565 not registered Live/Pending |
CESAR AUGUSTO OLSEN 2019-10-02 |
OLSEN 88015606 not registered Live/Pending |
Harbor Freight Tools USA, Inc. 2018-06-26 |
OLSEN 87907493 5789236 Live/Registered |
ECR International, Inc. 2018-05-04 |
OLSEN 87891064 5622577 Live/Registered |
ECR International, Inc. 2018-04-24 |
OLSEN 86069202 not registered Dead/Abandoned |
Kenneth A. Olsen 2013-09-19 |
OLSEN 79254197 not registered Dead/Abandoned |
Olsen Holding GmbH 2019-01-03 |
OLSEN 79253453 not registered Dead/Abandoned |
Olsen Holding GmbH 2019-01-28 |
OLSEN 79173460 4966940 Live/Registered |
Olsen Holding GmbH 2015-07-15 |
OLSEN 78571937 3225707 Dead/Cancelled |
Baugher, Jeffrey M. 2005-02-22 |
OLSEN 78459853 3313473 Dead/Cancelled |
SPECIALTY SURGICAL INSTRUMENTATION INC. 2004-07-30 |
OLSEN 76446875 3390498 Live/Registered |
SPECIALTY SURGICAL INSTRUMENTATION INC. 2002-09-03 |