Primary Device ID | 20845854044213 |
NIH Device Record Key | bf43f085-f521-435a-8b42-3ec4137a24b9 |
Commercial Distribution Discontinuation | 2023-03-09 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | HD5530RFB |
Catalog Number | HD5530RFB |
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 | true |
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 | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Outer Diameter | 5.5 Millimeter |
Angle | 30 degree |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10845854044216 [Primary] |
GS1 | 20845854044213 [Direct Marking] |
GCJ | Laparoscope, general & plastic surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
[20845854044213]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-03-09 |
Device Publish Date | 2016-10-14 |
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