Primary Device ID | 24053613291709 |
NIH Device Record Key | 56ad73db-0231-4cb5-87ba-d83084fe114b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ConMed® |
Version Model Number | DC089-064-35 |
Catalog Number | DC089-064-35 |
Company DUNS | 317409001 |
Company Name | Gebr. Brasseler GmbH & Co. KG |
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 | 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 14053613291702 [Primary] |
GS1 | 24053613291709 [Package] Contains: 14053613291702 Package: [5 Units] In Commercial Distribution |
GFA | Blade, Saw, General & Plastic Surgery, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-08 |
Device Publish Date | 2024-10-31 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CONMED 87743956 not registered Live/Pending |
ConMed Corporation 2018-01-04 |
CONMED 87551457 5467478 Live/Registered |
ConMed Corporation 2017-08-01 |
CONMED 87013011 5304308 Live/Registered |
ConMed Corporation 2016-04-25 |
CONMED 75292291 2213939 Live/Registered |
ConMed Corporation 1997-05-15 |
CONMED 73000298 1004240 Live/Registered |
CONSOLIDATED MEDICAL EQUIPMENT, INC. 1973-09-06 |