← Back to catalogue

PinPoint

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 187S

by Beekley Corporation

Identity

Trade Name
PinPoint® FDA UDI
Generic Name
Radiological image marker, noninvasive, single-use FDA UDI
Device Name
PinPoint EUDAMED
MRI Skin Markers for Small Field of View Imaging, 6mm Radiance filled inner diameter FDA UDI
Model / Reference
187S EUDAMEDFDA UDI
Description
MRI Skin Markers for Small Field of View Imaging, 6mm Radiance filled inner diameter FDA UDI

Identifiers

Primary DI / UDI-DI
00815137021503 EUDAMEDFDA UDI
Basic UDI-DI
00815137021503BE EUDAMED
FDA Product Code
JAC FDA UDI
EMDN Code
Z11030585 RADIOLOGY INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Radiological image marker, noninvasive, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
892.1640 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

PinPoint by Beekley Corporation — Class I — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Beekley Corporation
EUDAMED SRN
US-MF-000007055
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 6763f0c6-0eae-4abd-8466-c448edc24222 61 fields · synced Jul 21, 2026
  • FDA UDI 1c4860b1-6621-4f7a-a45f-91a4c0f82071 33 fields · synced May 30, 2026