AquaBeam 290010

GUDID 00748426127337

AQUABEAM® Robotic System Drape Set

Microtek Medical LLC

Medical equipment/instrument drape, single-use

• Primary Device ID: 00748426127337
• NIH Device Record Key: c583df0b-293d-4528-9b11-1ff53f16b631
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AquaBeam
• Version Model Number: Equipment Drapes
• Catalog Number: 290010
• Company DUNS: 106908437
• Company Name: Microtek Medical 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: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00748426127337 [Primary]

FDA Product Code

• PUI: Drape, Surgical, Exempt

Sterilization

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

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

[00748426127337]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-03-28
• Device Publish Date: 2025-03-11

On-Brand Devices [AquaBeam]

• 10748426127334: AQUABEAM® Robotic System Drape Set
• 00748426127337: AQUABEAM® Robotic System Drape Set