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Sunrise

FDA UDI

Class I (US FDA UDI)

by Tecan Austria GmbH

Identity

Trade Name
SUNRISE FDA UDI
Generic Name
Microplate reader IVD, automated/semi-automated FDA UDI
Device Name
microplate reader FDA UDI
Model / Reference
30087502 02 FDA UDI
Description
microplate reader FDA UDI

Identifiers

Catalog Number
30087502 FDA UDI
Primary DI / UDI-DI
09120052071184 FDA UDI
FDA Product Code
JJQ FDA UDI
GMDN Term
Microplate reader IVD, automated/semi-automated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2300 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: Microplate reader IVD, automated/semi-automated

Sunrise by Tecan Austria GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microplate reader IVD, automated/semi-automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tecan Austria GmbH

Sources (1)

  • FDA UDI a60a102f-e5ec-4b9c-8963-9287568c65e5 35 fields · synced May 31, 2026