INNERVUE SYSTEM 230 VOLT 922101

GUDID 00880304505995

Biomet Orthopedics, LLC

Rigid arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable

• Primary Device ID: 00880304505995
• NIH Device Record Key: 57057539-ffba-4770-a2ce-883cb91ccfe3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INNERVUE SYSTEM 230 VOLT
• Version Model Number: 922101
• Catalog Number: 922101
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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: true
• Serial Number: false
• Manufacturing Date: true
• 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)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304505995 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K040604

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

Moist Heat or Steam Sterilization

[00880304505995]

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: 2017-07-28

Devices Manufactured by Biomet Orthopedics, LLC

• 00887868004087 - PRIMARY TREPHINE: 2024-04-03
• 00887868004094 - BUSHING: 2024-04-03
• 00887868004100 - SECONDARY TREPHINE: 2024-04-03
• 00887868048272 - TREPHINE: 2024-04-03
• 00887868048289 - TREPHINE: 2024-04-03
• 00887868048296 - TREPHINE: 2024-04-03
• 00887868048302 - TREPHINE: 2024-04-03
• 00880304658387 - Compress®: 2024-03-11