DERMATOUCH

GUDID 00810169800249

Solid Wing Wholesale Inc.

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

• Primary Device ID: 00810169800249
• NIH Device Record Key: 58afbe67-1a0f-4a20-90b5-81275c629338
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DERMATOUCH
• Version Model Number: 81250MD/2XL
• Company DUNS: 118968508
• Company Name: Solid Wing Wholesale Inc.
• 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: 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	00810169800195 [Primary]
GS1	00810169800249 [Package]; Contains: 00810169800195; Package: CASE [10 Units]; In Commercial Distribution
GS1	10810169800192 [Unit of Use]

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: 2025-03-11
• Device Publish Date: 2025-03-03

On-Brand Devices [DERMATOUCH]

• 00810054146018: 81140/XXL
• 00810054146001: 81140/XL
• 00810054145998: 81140/L
• 00810054145981: 81140/M
• 00810054145974: 81140/S
• 00810054145967: 81140/XS
• 00810169800249: 81250MD/2XL
• 00810169800232: 81250MD/XL
• 00810169800225: 81250MD/L
• 00810169800218: 81250MD/M
• 00810169800201: 81250MD/S