Primary Device ID | 30845854032026 |
NIH Device Record Key | d5d79e6c-7434-49af-90c3-230b397d1d23 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | T4300 |
Catalog Number | T4300 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
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 |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Size Text, specify | 0 |
Angle | 30 degree |
Device Issuing Agency | Device ID |
---|---|
GS1 | 20845854032029 [Primary] |
GS1 | 30845854032026 [Direct Marking] |
HRX | ARTHROSCOPE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
[30845854032026]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-24 |
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