Identity
- Trade Name
- Member's Mark FDA UDI
- Generic Name
- Home-use/point-of-care blood glucose/blood pressure monitoring system FDA UDI
- Model / Reference
- 707001 FDA UDI
Identifiers
- Primary DI / UDI-DI
- MHC17070011 FDA UDI
- FDA Product Code
- NBW FDA UDI
- GMDN Term
- Home-use/point-of-care blood glucose/blood pressure monitoring system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1345 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
Member's Mark by Walmart Stores — Class II — 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.
- HealthPro — MHC Medical Products · Class II
- EasyTouch — MHC Medical Products · Class II
- EasyTouch — MHC Medical Products · Class II
- HealthPro — MHC Medical Products · Class II
- EasyTouch — MHC Medical Products · Class I
- Dario Blood Glucose Monitoring System — LABSTYLE INNOVATION LTD
- Member's Mark — Walmart Stores · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Walmart Stores
Sources (1)
- FDA UDI 267b70b4-3cbd-4fbb-b9b2-daa32fb7c9fd 32 fields · synced Jun 8, 2026