Identity
- Trade Name
- microINR ® Link Kit FDA UDI
- Generic Name
- Coagulation analyser IVD, home-use, battery-powered FDA UDI
- Model / Reference
- KTE0001AD FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08436540290908 FDA UDI
- 510(k) Number
- K231711 FDA UDI
- FDA Product Code
- GJS FDA UDI
- GMDN Term
- Coagulation analyser IVD, home-use, battery-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.7750 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
Yes
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
microINR ® Link Kit by Iline Microsystems Sl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K231711 also covers:
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 |
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Manufacturer
- Manufacturer
- Iline Microsystems Sl
Sources (1)
- FDA UDI c9fd33bf-149d-4304-b637-f8c21ed9fdd7 34 fields · synced May 30, 2026