HD4302

GUDID 30845854036000

4MM, 30 DEGREE HD QUICKLATCH AUTOCLAVABLE EYECUP SCOPE

Conmed Corporation

Rigid arthroscope, reusable

Primary Device ID	30845854036000
NIH Device Record Key	fc4ae27d-3fc6-45d6-8c15-73b8c44c9e0c
Commercial Distribution Status	In Commercial Distribution
Version Model Number	HD4302
Catalog Number	HD4302
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

Customer Support Contacts

Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM

Device Dimensions

Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree
Outer Diameter	4 Millimeter
Angle	30 degree

Operating and Storage Conditions

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
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 Identifiers

Device Issuing Agency	Device ID
GS1	20845854036003 [Primary]
GS1	30845854036000 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K962075

FDA Product Code

HRX	ARTHROSCOPE

Sterilization

Steralize Prior To Use	true
Device Is Sterile	false

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

[30845854036000]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	3
Public Version Date	2018-07-06
Device Publish Date	2016-09-24

Devices Manufactured by Conmed Corporation

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30653405987585 - PlumeSafe® X5™	2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit, 220V-240V 50/60 Hz
30653405987592 - PlumeSafe® X5™	2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit with PlumeSafe® X5™ Smoke Evacuator Filter, 220V-240V 50/60 Hz
30653405987608 - PlumeSafe® X5™	2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit, 220V-240V 50/60 Hz
30653405990141 - PlumeSafe® X5™	2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit with PlumeSafe® X5™ Smoke Evacuator Filter, 220V-240V 50/60 Hz
20653405990120 - BioBrace	2024-09-30 BioBrace® Reinforced Implant, 23 x 25 mm
20653405990137 - BioBrace	2024-09-30 BioBrace® Reinforced Implant, 35 x 25 mm

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