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Eonis DNA Extraction kit

FDA UDI

Class I (US FDA UDI)

by Wallac, Inc.

Identity

Trade Name
Eonis DNA Extraction kit FDA UDI
Generic Name
Nucleic acid extraction/isolation kit IVD FDA UDI
Device Name
The Eonis DNA Extraction kit is a device intended for isolation and purification of DNA in newborn blood specimens dried on filter paper. FDA UDI
Model / Reference
3240-001U FDA UDI
Description
The Eonis DNA Extraction kit is a device intended for isolation and purification of DNA in newborn blood specimens dried on filter paper. FDA UDI

Identifiers

Catalog Number
3240-001U FDA UDI
Primary DI / UDI-DI
06438147377718 FDA UDI
FDA Product Code
JJH FDA UDI
GMDN Term
Nucleic acid extraction/isolation kit IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2310 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Category: Nucleic acid extraction/isolation kit IVD

Eonis DNA Extraction kit by Wallac, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid extraction/isolation kit IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wallac, Inc.

Sources (1)

  • FDA UDI 2aaa12ca-8b59-4268-97c7-10739bff678c 35 fields · synced May 31, 2026