Insighter

GUDID 06970831725936

Shenzhen Insighters Medical Technology Co., Ltd.

Laryngeal mask airway, single-use

• Primary Device ID: 06970831725936
• NIH Device Record Key: 7e98ff68-8d95-4592-b1d9-b3a64276eec3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Insighter
• Version Model Number: iS-LMA-A 40
• Company DUNS: 551096917
• Company Name: Shenzhen Insighters Medical Technology Co., Ltd.
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970831725936 [Primary]

FDA Product Code

• CAE: Airway, Oropharyngeal, Anesthesiology

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: 2023-01-13
• Device Publish Date: 2023-01-05

On-Brand Devices [Insighter]

• 06970831725943: iS-LMA-A 50
• 06970831725936: iS-LMA-A 40
• 06970831725929: iS-LMA-A 30
• 06970831723390: Standard type 6Fr
• 16970831723342: i6-L
• 16970831723335: i6-M
• 16970831723328: i6-S
• 16970831723311: i6-SS
• 16970831723304: L
• 16970831723298: M
• 16970831723281: S
• 16970831723274: SS
• 06970831723192: iS3-C
• 06970831723154: iS3-F
• 06970831723017: insight ST1