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PrepIT L2P

EUDAMEDFDA UDI

Class A (EU MDR)

Ref PT-L2P-5

by DNA Genotek Inc.

Identity

Trade Name
PrepIT L2P EUDAMEDFDA UDI
Generic Name
Nucleic acid extraction/isolation kit IVD FDA UDI
Device Name
PrepIT L2P EUDAMED
DNA Preparation Kit, 5 ml FDA UDI
Model / Reference
PT-L2P-5 EUDAMEDFDA UDI
Description
DNA Preparation Kit, 5 ml FDA UDI

Identifiers

Catalog Number
PT-L2P-5 FDA UDI
Primary DI / UDI-DI
00627595000415 EUDAMEDFDA UDI
Basic UDI-DI
0627595H0800HX EUDAMED
FDA Product Code
PPM FDA UDI
EMDN Code
W01019099 CLINICAL CHEMISTRY REAGENTS - OTHER EUDAMED
GMDN Term
Nucleic acid extraction/isolation kit IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.4010 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

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

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

PrepIT L2P by DNA Genotek Inc — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid extraction/isolation kit IVD.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DNA Genotek Inc.
EUDAMED SRN
CA-MF-000003486
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (2)

  • EUDAMED c163602e-2305-4c8a-aa10-5aaf0d3834bd 61 fields · synced Jul 10, 2026
  • FDA UDI b185995c-6897-4ab1-adac-c5f4dd7f325f 36 fields · synced May 30, 2026