← Back to catalogue

Protonion™ 96 Viral RNA Kit

FDA UDI

Class I (US FDA UDI)

by Bioneer Corporation

Identity

Trade Name
Protonion™ 96 Viral RNA Kit FDA UDI
Generic Name
Nucleic acid extraction/isolation kit IVD FDA UDI
Device Name
384 test/kit FDA UDI
Model / Reference
K-4731 FDA UDI
Description
384 test/kit FDA UDI

Identifiers

Catalog Number
K-4731 FDA UDI
Primary DI / UDI-DI
08809537070461 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nucleic acid extraction/isolation kit IVD

Protonion™ 96 Viral RNA Kit by Bioneer Corporation — 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

Manufacturer
Bioneer Corporation

Sources (1)

  • FDA UDI dc37b32c-6c41-4b11-b4f1-522a0b47cef8 34 fields · synced May 30, 2026