MST 0.9 Bent Mini A1 12° 30° PT-32130-P-1

GUDID 00844685003532

MICROSURGICAL TECHNOLOGY, INC.

Phacoemulsification system handpiece tip, reusable

• Primary Device ID: 00844685003532
• NIH Device Record Key: 31e79dc2-3a11-4c76-a4e2-4ea9fcfb9064
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MST 0.9 Bent Mini A1 12° 30°
• Version Model Number: PT-32130-P-1
• Catalog Number: PT-32130-P-1
• Company DUNS: 097824130
• Company Name: MICROSURGICAL TECHNOLOGY, INC.
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00844685003532 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K943672

FDA Product Code

• HQC: Unit, Phacofragmentation

Sterilization

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

[00844685003532]

Radiation Sterilization;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: 2016-11-14

On-Brand Devices [MST 0.9 Bent Mini A1 12° 30°]

• 00844685003549: PT-32130-R-1
• 00844685003532: PT-32130-P-1