Primary Device ID | 20845854024192 |
NIH Device Record Key | ac0c33f0-72f8-49d3-8182-9b1919ad3af0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ULTRAFIX |
Version Model Number | 10121 |
Catalog Number | 10121 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
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(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10845854024195 [Primary] |
GS1 | 20845854024192 [Direct Marking] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
[20845854024192]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-09-28 |
Device Publish Date | 2020-09-24 |
30845854037144 | ULTRAFIX MICROMITE DRILL, 1.8MM |
30845854037113 | ULTRAFIX ARTHROSCOPIC DRILL, 2.4MM |
30845854037106 | ULTRAFIX DRILL, 2.4MM |
30845854037076 | ULTRAFIX ARTHROSCOPIC DRILL GUIDE |
30845854037021 | ULTRAFIX DRILL 3.2MM |
30845854037014 | ULTRAFIX DRILL GUIDE |
30845854024199 | ULTRAFIX ARTHROSCOPIC INSERTER |
20845854024192 | ULTRAFIX ARTHROSCOPIC INSERTER |
20845854037062 | ULTRAFIX ARTHROSCOPIC DRILL, 3.2MM |
20845854037024 | ULTRAFIX DRILL 3.2MM |
20845854037116 | ULTRAFIX ARTHROSCOPIC DRILL, 2.4 MM |
20845854037109 | ULTRAFIX DRILL, 2.4 MM |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ULTRAFIX 98542329 not registered Live/Pending |
ULTRAFIX APPLIANCE PARTS LLC 2024-05-09 |
ULTRAFIX 98525541 not registered Live/Pending |
9485-7489 Quebec Inc. 2024-04-29 |
ULTRAFIX 78031285 2494514 Dead/Cancelled |
Green, Tommy Joe O. 2000-10-18 |
ULTRAFIX 75003610 2162402 Live/Registered |
CONMED CORPORATION 1995-10-03 |
ULTRAFIX 74380431 1887717 Live/Registered |
EK Industries, Inc. 1993-04-15 |
ULTRAFIX 72051855 0702059 Dead/Cancelled |
Brown-Forman Distillers Corporation 1958-05-19 |
ULTRAFIX 71666887 0600232 Dead/Expired |
VERONA CHEMICAL COMPANY 1954-05-21 |