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EasyTouch

FDA UDI

Class I (US FDA UDI)

by MHC Medical Products

Identity

Trade Name
EasyTouch FDA UDI
Generic Name
Home-use/point-of-care blood glucose/blood pressure monitoring system FDA UDI
Model / Reference
810001 FDA UDI

Identifiers

Primary DI / UDI-DI
MHC18100012 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Home-use/point-of-care blood glucose/blood pressure monitoring system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Home-use/point-of-care blood glucose/blood pressure monitoring system

EasyTouch by MHC Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home-use/point-of-care blood glucose/blood pressure monitoring system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ff26f68-cae0-46f5-a7a6-8b06ef26ebed 32 fields · synced May 30, 2026