RAPIDFLAP (TM) SYSTEM 75-1013

GUDID 00841036071042

BIOMET MICROFIXATION, INC

Bone holding forceps

• Primary Device ID: 00841036071042
• NIH Device Record Key: b649dc7a-628c-4b9f-990d-c8607a7da712
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RAPIDFLAP (TM) SYSTEM
• Version Model Number: 75-1013
• Catalog Number: 75-1013
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, INC
• 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(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841036071042 [Primary]

FDA Product Code

• HTD: FORCEPS

Sterilization

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

[00841036071042]

Moist Heat or Steam Sterilization

[00841036071042]

Moist Heat or Steam Sterilization

[00841036071042]

Moist Heat or Steam Sterilization

[00841036071042]

Moist Heat or Steam Sterilization

[00841036071042]

Moist Heat or Steam Sterilization

[00841036071042]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-08-21
• Device Publish Date: 2018-09-14

On-Brand Devices [RAPIDFLAP (TM) SYSTEM]

• 00841036142049: 75-1040-12
• 00841036142032: 75-1030-12
• 00841036142025: 75-1020-12
• 00841036071042: 75-1013
• 00841036068028: 75-1040
• 00841036065492: 75-1030
• 00841036061296: 75-1011
• 00841036058586: 75-1020
• 00888233011273: 75-1040-12
• 00888233011259: 75-1030-12
• 00888233011235: 75-1020-12