Identity
- Trade Name
- EUROStar IV Plus FDA UDI
- Generic Name
- Fluorescence light microscope IVD FDA UDI
- Model / Reference
- YG 0307-0101 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04049016159025 FDA UDI
- FDA Product Code
- KEI FDA UDI
- GMDN Term
- Fluorescence light microscope IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.3600 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Fluorescence light microscope IVD
EUROStar IV Plus by EUROIMMUN Medizinische Labordiagnostika AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Fluorescence light microscope IVD.
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 I | Pending data |
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Manufacturer
- Manufacturer
- EUROIMMUN Medizinische Labordiagnostika AG
Sources (1)
- FDA UDI 32787b55-101f-4de6-bee8-70d613138736 32 fields · synced Jun 8, 2026