Litetouch

GUDID 00840216123472

LITETOUCH LANCING DEVICE (DOLPHIN) - 1/EA, 1EA/BX, 100BX/IC, 4IC/MCS (400EA)

Asp Global, LLC

Manual blood lancing device, reusable

• Primary Device ID: 00840216123472
• NIH Device Record Key: d7dd5377-6c98-41ff-9132-92879614f2b2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Litetouch
• Version Model Number: 20PS-BL
• Company DUNS: 080361159
• Company Name: Asp Global, LLC
• Device Count: 1
• 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: false
• Lot Batch: true
• 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	00840216123465 [Primary]
GS1	00840216123472 [Package]; Contains: 00840216123465; Package: Inner Box [1 Units]; In Commercial Distribution
GS1	10840216123462 [Package]; Contains: 00840216123465; Package: Inner Case [100 Units]; In Commercial Distribution
GS1	20840216123469 [Package]; Contains: 00840216123465; Package: Master Case [400 Units]; In Commercial Distribution

FDA Product Code

• QRK: Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

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: 2023-11-24
• Device Publish Date: 2023-11-16

On-Brand Devices [Litetouch]

• 00840216124332: LITE TOUCH MICRO THIN LANCETS - 33G - 1/EA, 100EA/BX, 100BX/CS (10000EA)
• 00840216124318: LITE TOUCH ULTRA THIN LANCETS - 30G - 1/EA, 100EA/BX, 100BX/CS (10000EA)
• 00840216123472: LITETOUCH LANCING DEVICE (DOLPHIN) - 1/EA, 1EA/BX, 100BX/IC, 4IC/MCS (400EA)