← Back to catalogue

Dakota™

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref M0063905000

by Boston Scientific Corporation

Identity

Trade Name
DAKOTA™ EUDAMED
DAKOTA FDA UDI
Generic Name
Urinary stone retrieval basket, single-use FDA UDI
Device Name
Dakota™ Nitinol Stone Retrieval Device with OpenSure™ Handle EUDAMED
Nitinol Stone Retrieval Device FDA UDI
Model / Reference
M0063905000 EUDAMEDFDA UDI
Description
Nitinol Stone Retrieval Device FDA UDI

Identifiers

Primary DI / UDI-DI
08714729937364 EUDAMEDFDA UDI
Basic UDI-DI
01915060000000000000273N5 EUDAMED
FDA Product Code
FFL FDA UDI
EMDN Code
U090101 URINARY STONE RETRIEVAL BASKETS EUDAMED
GMDN Term
Urinary stone retrieval basket, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.4680 FDA UDI
Market of Registration
Netherlands 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dakota™ by Boston Scientific Corporation — 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

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

Manufacturer

EUDAMED SRN
US-MF-000004702
Authorised Representative
Boston Scientific Limited IE-AR-000003840

Sources (2)

  • EUDAMED ca616ccc-d3db-4ef7-b806-0fca149382db 61 fields · synced Jun 19, 2026
  • FDA UDI 37ff2223-bad2-45e0-8fb4-b148fd119cbe 34 fields · synced May 30, 2026