GII 213207

GUDID 10886705002610

Slotted Drill Guide GII / SUPER / RC / GLS

DEPUY MITEK, LLC

Manual surgical rotary handpiece, reusable

• Primary Device ID: 10886705002610
• NIH Device Record Key: fae16646-778a-4cab-b6a6-d722861d3734
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GII
• Version Model Number: 213207
• Catalog Number: 213207
• Company DUNS: 190572854
• Company Name: DEPUY MITEK, 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886705002610 [Primary]

FDA Product Code

• FZX: Guide, surgical, instrument

Sterilization

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

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

[10886705002610]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-09-20
• Device Publish Date: 2015-09-01

On-Brand Devices [GII]

• 10886705003761: Gll Arthroscopic Inserter
• 10886705001910: GII Inserter
• 10886705000975: GII Anchor Threader Tab
• 10886705002610: Slotted Drill Guide GII / SUPER / RC / GLS
• 10886705001743: Arthroscopic GII Drill Bit 2.4mm
• 10886705001576: GII Drill Bit 2.4mm
• 20886705000941: GII Anchor Threader Tab