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ExiPrep™16 Plus

FDA UDI

Class I (US FDA UDI)

by Bioneer Corporation

Identity

Trade Name
ExiPrep™16 Plus FDA UDI
Generic Name
Nucleic acid sample preparation instrument IVD FDA UDI
Model / Reference
A-5030 FDA UDI

Identifiers

Primary DI / UDI-DI
08809537077750 FDA UDI
FDA Product Code
JJH FDA UDI
GMDN Term
Nucleic acid sample preparation instrument 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

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: Nucleic acid sample preparation instrument IVD

ExiPrep™16 Plus by Bioneer Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bioneer Corporation

Sources (1)

  • FDA UDI c5a61832-58b3-401c-8dca-b913c6a530d4 32 fields · synced May 30, 2026