ProTrap Luma

GUDID 00858276007922

ProTrap-Luma In-Line Polyp Trap

Micro-tech Usa

Surgical suction system collection container, single-use

• Primary Device ID: 00858276007922
• NIH Device Record Key: 8b3d8985-2469-4223-8378-4e32883dce9d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProTrap Luma
• Version Model Number: BBPA00001
• Company DUNS: 079873914
• Company Name: Micro-tech Usa
• Device Count: 1
• DM Exempt: true
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	00858276007915 [Primary]
GS1	00858276007922 [Package]; Contains: 00858276007915; Package: Box [25 Units]; In Commercial Distribution
GS1	00858276007939 [Package]; Package: Case [8 Units]; In Commercial Distribution

FDA Product Code

• KDQ: Bottle, Collection, Vacuum

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-03-11
• Device Publish Date: 2025-03-03

On-Brand Devices [ProTrap Luma]

• 00858276007953: ProTrap-Luma Polyp Trap Specimen Tray
• 00858276007922: ProTrap-Luma In-Line Polyp Trap