← Back to catalogue
GLUCOCARD® Expression™ Blood Glucose Monitoring System
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- GLUCOCARD® Expression™ Blood Glucose Monitoring System FDA UDI
- Generic Name
- Glucose monitoring system IVD, home-use FDA UDI
- Device Name
- DME: Startup Portable Blood Glucose Meter System. Includes: meter, test strips, IFU FDA UDI
- Model / Reference
- 571188 FDA UDI
- Description
- DME: Startup Portable Blood Glucose Meter System. Includes: meter, test strips, IFU FDA UDI
Identifiers
- Primary DI / UDI-DI
- 30015482571888 FDA UDI
- FDA Product Code
- NBW FDA UDICGA FDA UDI
- GMDN Term
- Glucose monitoring system IVD, home-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1345 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
GLUCOCARD® Expression™ Blood Glucose Monitoring System by Arkray Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Arkray Usa, Inc.
Sources (1)
- FDA UDI 5201cb84-0afc-4aa8-8c9d-0c3134acb324 36 fields · synced May 30, 2026