Primary Device ID | 20845854024871 |
NIH Device Record Key | 9ab735ab-a1f7-4431-9de0-6648c446914b |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 8191-01 |
Catalog Number | 8191-01 |
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 | 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(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00845854024877 [Primary] |
GS1 | 20845854024871 [Direct Marking] |
FET | Endoscopic video imaging system/component, gastroenterology-urology |
Steralize Prior To Use | true |
Device Is Sterile | false |
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
[20845854024871]
Moist Heat or Steam Sterilization;Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-24 |
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30845854034617 - GENESYS CrossFT, Hi-Fi | 2024-04-25 GENESYS CrossFT 6.5 mm Suture Anchor, w/2 Hi-Fi #2 (5 metric) Sutures w/Needles |
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