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384-Well Spectral Calibration Plate 1, a part of 384-Well 10-Dye Spectral Calib…
EUDAMEDFDA UDIClass A (EU MDR)
Ref A52439 (A52523)
Identity
- Trade Name
- 384-Well Spectral Calibration Plate 1, a part of 384-Well 10-Dye Spectral Calibration Plate EUDAMED384-Well Spectral Calibration Plate 1 FDA UDI
- Generic Name
- Optical laboratory instrument performance standard calibrator/control IVD, single-use FDA UDI
- Device Name
- Spectral Calibration Plates, a part of Calibration and Verification Plates EUDAMED
- Model / Reference
- A52439 (A52523) EUDAMEDA52439 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10190302016940 EUDAMEDFDA UDI
- Basic UDI-DI
- 0190302TCF0000576BAM EUDAMED
- FDA Product Code
- OOI FDA UDI
- EMDN Code
- W02050199 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - OTHER EUDAMED
- GMDN Term
- Optical laboratory instrument performance standard calibrator/control IVD, single-use FDA UDI
Classification
- Device Class
- Class A EUDAMEDClass II FDA UDI
- Regulation Number
- 862.2570 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
Yes
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
384-Well Spectral Calibration Plate 1, a part of 384-Well 10-Dye Spectral Calib… by Life Technologies Holdings Pte Ltd. — Class A — IVDR, FDA UDI — listed in…
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 0190302TCF0000576BAM | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
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Manufacturer
- Manufacturer
- Life Technologies Holdings Pte Ltd
- EUDAMED SRN
- SG-MF-000023931
- Authorised Representative
- Life Technologies Europe B.V. NL-AR-000021890
Sources (2)
- EUDAMED 2fa0dc07-5907-4235-8f00-befafcad49ca 61 fields · synced Jun 19, 2026
- FDA UDI 93fceb18-af1d-40ad-b501-ef34172f6cad 32 fields · synced May 30, 2026