Identity
- Trade Name
- HemoCue® Hb 201 Microcuvettes FDA UDI
- Generic Name
- Haemoglobin analyser IVD, point-of-care FDA UDI
- Device Name
- HemoCue Hb 201 Microcuvettes 4x50 vial FDA UDI
- Model / Reference
- 111716 FDA UDI
- Description
- HemoCue Hb 201 Microcuvettes 4x50 vial FDA UDI
Identifiers
- Catalog Number
- 111716 FDA UDI
- Primary DI / UDI-DI
- 17311091117165 FDA UDI
- 510(k) Number
- K032203 FDA UDI
- FDA Product Code
- GKR FDA UDI
- GMDN Term
- Haemoglobin analyser IVD, point-of-care FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.5620 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
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Haemoglobin analyser IVD, point-of-care
HemoCue® Hb 201 Microcuvettes by Hemocue, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Haemoglobin analyser IVD, point-of-care.
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- Mission Plus Hemoglobin (Hb) Monitoring System — ACON Laboratories, Inc. · Class II
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Cleared under the same submission
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
- Hemocue, Inc.
Sources (1)
- FDA UDI 08c7135f-4d45-4faf-9bfd-87aefbdfff5d 36 fields · synced May 30, 2026