Mia Secret

GUDID 00842342116700

MIA SECRET

Nitrile examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 00842342116700
• NIH Device Record Key: b031712a-2cd3-4801-bc2c-332e9ba5e679
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mia Secret
• Version Model Number: NGL-1215
• Company DUNS: 118924410
• Company Name: MIA SECRET
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Manufacturing Date: true
• Expiration Date: true
• 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	00842342116557 [Primary]
GS1	00842342116700 [Package]; Contains: 00842342116557; Package: [10 Units]; In Commercial Distribution
GS1	30842342116558 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133307

FDA Product Code

• LZA: Polymer Patient Examination Glove

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: 2023-03-15
• Device Publish Date: 2023-03-07

On-Brand Devices [Mia Secret]

• 00842342116717: NGXL-1220
• 00842342116700: NGL-1215
• 00842342116694: NGM-1210
• 00842342116687: NGS-1205