MedtLancet 30-22-2818

GUDID M992302228185

Safety lancet 28G*1.8mm

Carelife (usa) Inc.

Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use

• Primary Device ID: M992302228185
• NIH Device Record Key: 4bc1e618-ebbd-4aa7-bafc-49c34979b7ff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MedtLancet
• Version Model Number: 1
• Catalog Number: 30-22-2818
• Company DUNS: 065756949
• Company Name: Carelife (usa) 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: 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com
• Phone: 7709356499
• Email: li@carelifeusa.com

Device Dimensions

• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M992302228180 [Unit of Use]
HIBCC	M992302228183 [Primary]
HIBCC	M992302228185 [Package]; Contains: M992302228183; Package: corrugate carton [20 Units]; In Commercial Distribution

FDA Product Code

• FMK: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

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: 2023-11-09
• Device Publish Date: 2023-11-01

On-Brand Devices [MedtLancet]

• M992302228185: Safety lancet 28G*1.8mm
• M992302226185: Safety lancet 26G*1.8mm