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HighPrep PCR - DX (500 mL)

EUDAMEDFDA UDI

Class A (EU MDR)

Ref AC-60500EModel Device for post-PCR and post-enzymatic reaction clean-up

by MagBio Genomics, Inc.

Identity

Trade Name
HighPrep PCR - DX (500 mL) EUDAMED
MagBio Genomics, Inc. FDA UDI
Generic Name
Nucleic acid library construction kit IVD FDA UDI
Device Name
HighPrep PCR - DX (500 mL) EUDAMED
Post-PCR and post-enzymatic reaction clean-up FDA UDI
Model / Reference
Device for post-PCR and post-enzymatic reaction clean-up EUDAMED
AC-60500E EUDAMED
HighPrep™ PCR FDA UDI
Description
Post-PCR and post-enzymatic reaction clean-up FDA UDI

Identifiers

Catalog Number
AC-60500 FDA UDI
Primary DI / UDI-DI
00850045030155 EUDAMEDFDA UDI
Basic UDI-DI
0850045030AC-60500EA6 EUDAMED
Direct Marketing DI
00850045030155 EUDAMED
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED
GMDN Term
Nucleic acid library construction kit IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nucleic acid sample preparation instrument IVD

HighPrep PCR - DX (500 mL) by MagBio Genomics, Inc. — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000038221
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (2)

  • EUDAMED 4d386a82-e878-4f8b-98ad-d1a8a4fc670f 61 fields · synced Jul 20, 2026
  • FDA UDI 2709dadf-932a-4d56-bcbb-4eb7ab6f8c9a 35 fields · synced May 30, 2026