Surelife

GUDID MHC18602122

MHC MEDICAL PRODUCTS, LLC

Manual-inflation electronic sphygmomanometer, portable

• Primary Device ID: MHC18602122
• NIH Device Record Key: 9f4d0c11-91ad-4562-a2ca-03052c10d035
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Surelife
• Version Model Number: 860212
• Company DUNS: 169895245
• Company Name: MHC MEDICAL PRODUCTS, 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: 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
HIBCC	MHC18602122 [Primary]

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-11-08
• Device Publish Date: 2016-08-05

On-Brand Devices [Surelife]

• MHC18602142: 860214
• MHC18602132: 860213
• MHC18602122: 860212
• MHC18602112: 860211
• MHC18603203: 860320
• MHC18603103: 860310