Tourniquet System 40800

GUDID 06975218190239

Anetic Aid USA LLC

Tourniquet cuff, single-use

• Primary Device ID: 06975218190239
• NIH Device Record Key: 50ffe5b3-bf91-4dac-953e-f7af76bf08c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tourniquet System
• Version Model Number: Single-use Sterile Tourniquet Cuff - Pediatric
• Catalog Number: 40800
• Company DUNS: 083649158
• Company Name: Anetic Aid USA 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: true
• Lot Batch: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06975218190239 [Primary]

FDA Product Code

• KCY: Tourniquet, Pneumatic

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: 2023-09-19
• Device Publish Date: 2023-09-11

On-Brand Devices [Tourniquet System]

• 06975218190352: Single-use Sterile Tourniquet Cuff - Large Leg - C
• 06975218190338: Single-use Sterile Tourniquet Cuff - Large Leg
• 06975218190314: Single-use Sterile Tourniquet Cuff - Leg - Conical
• 06975218190291: Single-use Sterile Tourniquet Cuff - Large Arm / S
• 06975218190277: Single-use Sterile Tourniquet Cuff - Arm
• 06975218190253: Single-use Sterile Tourniquet Cuff - Leg
• 06975218190239: Single-use Sterile Tourniquet Cuff - Pediatric
• 05060228640537: AT4 Electronic Tourniquet