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goldFISH

FDA UDI

Class I (US FDA UDI)

by Lumatas Biosystems, Inc.

Identity

Trade Name
goldFISH FDA UDI
Generic Name
Assay development analyte-specific reagent IVD FDA UDI
Device Name
MYB Dual Color Break Apart Probe FDA UDI
Model / Reference
DF073 FDA UDI
Description
MYB Dual Color Break Apart Probe FDA UDI

Identifiers

Primary DI / UDI-DI
00810202560208 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Assay development analyte-specific reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4020 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assay development analyte-specific reagent IVD

goldFISH by Lumatas Biosystems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assay development analyte-specific reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7396e308-554c-425a-96bd-4a313c8230c5 35 fields · synced May 30, 2026