← Back to catalogue

EchoLUTION Viral RNA/DNA Kit (8 x 96)

FDA UDI

Class I (US FDA UDI)

by BioEcho Life Sciences GmbH

Identity

Trade Name
EchoLUTION Viral RNA/DNA Kit (8 x 96) FDA UDI
Generic Name
Nucleic acid extraction/isolation kit IVD FDA UDI
Model / Reference
012-102-008-Dx FDA UDI

Identifiers

Catalog Number
012-102-008-Dx FDA UDI
Primary DI / UDI-DI
04260759850219 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

Yes

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

EchoLUTION Viral RNA/DNA Kit (8 x 96) by BioEcho Life Sciences GmbH — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 65f773a0-d8ee-4ef0-9f42-8953773e4586 33 fields · synced May 30, 2026