Primary Device ID | 07640143933211 |
NIH Device Record Key | de37671c-f334-46fa-b75f-e4bc0f7d4a83 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | schaerer® arcus |
Version Model Number | 92427 |
Catalog Number | 92427 |
Company DUNS | 484713792 |
Company Name | Schaerer Medical AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640143933211 [Primary] |
FQO | Table, Operating-Room, Ac-Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-11 |
Device Publish Date | 2023-07-03 |
07640143933211 | schaerer® arcus 8601 |
07640143931460 | schaerer® arcus 8501 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SCHAERER 79975007 not registered Dead/Abandoned |
Belimed AG 2005-06-02 |
SCHAERER 79975006 not registered Dead/Abandoned |
Belimed AG 2005-08-16 |
SCHAERER 79222158 5771967 Live/Registered |
Schaerer AG 2017-05-19 |
SCHAERER 79150877 4879000 Live/Registered |
Schaerer AG 2014-02-25 |
SCHAERER 79122667 4476478 Live/Registered |
Schaerer Medical Management AG 2012-11-23 |
SCHAERER 79017658 not registered Dead/Abandoned |
Schaerer Medical Management AG 2005-08-16 |
SCHAERER 79012965 3272496 Dead/Cancelled |
Schaerer Medical Management AG 2005-06-02 |
SCHAERER 78565370 3205038 Live/Registered |
SCHAERER AG 2005-02-11 |
SCHAERER 72467141 0997008 Dead/Expired |
MAUSER-SCHAERER G.M.B.H. 1973-08-31 |