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96‑Well 0.2‑mL Spectral Calibration Plate 3, a part of 96-Well 0.2 mL Spectral …

EUDAMEDFDA UDI

Class A (EU MDR)

Ref A31909 (A31888)

by Life Technologies Holdings Pte Ltd

Identity

Trade Name
96‑Well 0.2‑mL Spectral Calibration Plate 3, a part of 96-Well 0.2 mL Spectral Calibration Plate EUDAMED
96-Well 0.2-mL Calibration Plate 3 (TAMRA, NED, and Cy 5 dyes) 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
A31909 (A31888) EUDAMED
A31909 FDA UDI

Identifiers

Primary DI / UDI-DI
10190302003353 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 EUDAMED
Class 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

96‑Well 0.2‑mL Spectral Calibration Plate 3, a part of 96-Well 0.2 mL Spectral … 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

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Manufacturer

EUDAMED SRN
SG-MF-000023931
Authorised Representative
Life Technologies Europe B.V. NL-AR-000021890

Sources (2)

  • EUDAMED f38979d9-6b7f-4036-9aea-cd4f6c8d0a09 61 fields · synced Jun 18, 2026
  • FDA UDI f02b6769-90f2-4fb1-b9a5-fb62909a931a 32 fields · synced May 26, 2026