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AprioCore plus 18G, 19.5 cm

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref ACP18-195-20

by AprioMed AB

Identity

Trade Name
AprioCore plus 18G, 19.5 cm EUDAMED
AprioCore plus FDA UDI
Generic Name
Side-notch biopsy gun handpiece/needle FDA UDI
Device Name
AprioCore EUDAMED
AprioCore plus is a sterile, disposable, semi-automatic, spring-loaded biopsy needle. FDA UDI
Model / Reference
ACP18-195-20 EUDAMEDFDA UDI
Description
AprioCore plus is a sterile, disposable, semi-automatic, spring-loaded biopsy needle. FDA UDI

Identifiers

Catalog Number
ACP18-195-20 FDA UDI
Primary DI / UDI-DI
07350031350104 EUDAMEDFDA UDI
Basic UDI-DI
73500313510KE EUDAMED
510(k) Number
K193268 FDA UDI
FDA Product Code
KNW FDA UDI
EMDN Code
A0102010101 SHEARING BIOPSY NEEDLES EUDAMED
GMDN Term
Side-notch biopsy gun handpiece/needle FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.1075 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 19.5 Centimeter FDA UDI
Needle Gauge — 18 Gauge FDA UDI

AprioCore plus 18G, 19.5 cm by Apriomed AB — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AprioMed AB
EUDAMED SRN
SE-MF-000001013

Sources (2)

  • EUDAMED 380477e1-349b-4808-9343-525457f9f803 61 fields · synced Jun 19, 2026
  • FDA UDI a805ad19-fb57-49a4-b2ce-a71e52528de4 37 fields · synced May 30, 2026