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800ts

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 800TSI-SIModel 800TS-SI

by Agilent Technologies, Inc.

Identity

Trade Name
800TS EUDAMED
800TSI-SI FDA UDI
Generic Name
Microplate reader IVD, automated/semi-automated FDA UDI
Device Name
800TS EUDAMED
Absorbance Microplate Reader FDA UDI
Model / Reference
800TS-SI EUDAMED
800TSI-SI EUDAMEDFDA UDI
Description
Absorbance Microplate Reader FDA UDI

Identifiers

Primary DI / UDI-DI
05700574034269 EUDAMEDFDA UDI
Basic UDI-DI
5700570000000000A0300015Y EUDAMED
FDA Product Code
JJQ FDA UDI
EMDN Code
W0299 IVD INSTRUMENTS - OTHER EUDAMED
GMDN Term
Microplate reader IVD, automated/semi-automated FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
862.2300 FDA UDI
Market of Registration
Denmark 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

No

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

Yes

EUDAMED

New Device

No

EUDAMED

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

800ts by Agilent Technologies, Inc. — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000009385
Authorised Representative
Agilent Technologies Denmark ApS DK-AR-000001443

Sources (2)

  • EUDAMED a9b54dd9-7ecf-4acd-bc66-370554509ee3 61 fields · synced Jun 18, 2026
  • FDA UDI e209a3f0-e963-4def-924f-8fb3914ab185 35 fields · synced May 30, 2026