Comprehensive® Reverse Shoulder 110040301

GUDID 00887868254451

Biomet Orthopedics, LLC

Surgical screwdriver, reusable

• Primary Device ID: 00887868254451
• NIH Device Record Key: a5c83043-4ce8-4cf8-bccd-fa77eccf915f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Comprehensive® Reverse Shoulder
• Version Model Number: 110040301
• Catalog Number: 110040301
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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

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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868254451 [Primary]

FDA Product Code

• HXX: SCREWDRIVER

Sterilization

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

[00887868254451]

Moist Heat or Steam Sterilization

[00887868254451]

Moist Heat or Steam Sterilization

[00887868254451]

Moist Heat or Steam Sterilization

[00887868254451]

Moist Heat or Steam Sterilization

[00887868254451]

Moist Heat or Steam Sterilization

[00887868254451]

Moist Heat or Steam Sterilization

[00887868254451]

Moist Heat or Steam Sterilization

[00887868254451]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-21
• Device Publish Date: 2024-11-13

On-Brand Devices [Comprehensive® Reverse Shoulder]

• 00880304993259: 110032430
• 00880304993242: 110032420
• 00880304993235: 110032410
• 00880304993228: 110031869
• 00880304811324: 110029768
• 00880304811317: 110040130
• 00880304811300: 110040120
• 00880304811294: 110040110
• 00880304811287: 110029096
• 00880304811270: 110029095
• 00880304811263: 110029094
• 00880304811256: 110029093
• 00880304811249: 110029092
• 00880304811232: 110029091
• 00880304811225: 110040030
• 00880304811218: 110040020
• 00880304811201: 110040010
• 00880304811195: 110040201
• 00880304811188: 110040430
• 00880304811171: 110040420
• 00880304811164: 110040410
• 00880304811157: 110040530
• 00880304811140: 110040520
• 00880304811133: 110040510
• 00880304811126: 110040600
• 00880304811119: 110040200
• 00880304810952: 110040300
• 00880304810945: 110040230
• 00880304810938: 110040220
• 00880304810921: 110040210
• 00887868254529: 110040600
• 00887868254444: 110040201
• 00887868254437: 110040200
• 00887868254369: 110029096
• 00887868254352: 110029095
• 00887868254345: 110029094
• 00887868254338: 110029093
• 00887868254321: 110029092
• 00887868254314: 110029091
• 00887868254550: 110040230
• 00887868254543: 110040220
• 00887868254536: 110040210
• 00887868254512: 110040530
• 00887868254505: 110040520
• 00887868254499: 110040510
• 00887868254482: 110040430
• 00887868254475: 110040420
• 00887868254468: 110040410
• 00887868254420: 110040130
• 00887868254413: 110040120