TeleRPM / Chronica

GUDID 00850042929230

Lancing Device

Mio Labs Inc.

Manual blood lancing device, reusable

• Primary Device ID: 00850042929230
• NIH Device Record Key: e7ac5f16-8506-490b-8b28-7d324742be89
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TeleRPM / Chronica
• Version Model Number: HH-XIII-T
• Company DUNS: 117119317
• Company Name: Mio Labs Inc.
• 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: true
• 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	00850042929230 [Primary]

FDA Product Code

• QRL: Multiple Use Blood Lancet For Single Patient Use Only

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

On-Brand Devices [TeleRPM / Chronica]

• 00850042929230: Lancing Device
• 00850042929223: Single Use Lancets
• 00850042929216: TeleRPM Control Solution
• 00850042929247: TeleRPM Blood Glucose Monitoring System
• 00850042929209: TeleRPM Blood Glucose Test Strip
• 00850042929193: TeleRPM Blood Glucose Meter