Acquire Med 096657

GUDID 02816901023448

ACQUIRE MED

Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use

• Primary Device ID: 02816901023448
• NIH Device Record Key: f3a845db-dd67-4fc4-bd49-69499daaeeab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Acquire Med
• Version Model Number: Q-940-RT
• Catalog Number: 096657
• Company DUNS: 061766352
• Company Name: ACQUIRE MED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816901023440 [Primary]
GS1	01816901023449 [Package]; Contains: 00816901023440; Package: [5 Units]; In Commercial Distribution
GS1	02816901023448 [Package]; Contains: 01816901023449; Package: [2 Units]; In Commercial Distribution

FDA Product Code

• GEX: Powered laser surgical instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-05
• Device Publish Date: 2023-05-26

On-Brand Devices [Acquire Med]

• 01816901022855: Q-200-RT
• 02816901022847: Q-550-RT
• 01816901022831: Q-940-RT
• 02816901022823: Q-365-RT
• 02816901022984: Q-550-RTR
• 02816901023448: Q-940-RT