← Back to catalogue

Fusion Quattro Extraction Balloon

EUDAMEDFDA UDI

Class I (EU MDR)

Ref FS-QEB-B

by Wilson-Cook Medical, Inc.

Identity

Trade Name
Fusion Quattro Extraction Balloon EUDAMED
Fusion Quattro FDA UDI
Generic Name
ERCP catheter, balloon, non-electrical, stone-retrieval FDA UDI
Device Name
Fusion Quattro Extraction Balloon EUDAMEDFDA UDI
Model / Reference
FS-QEB-B EUDAMED
G48226 FDA UDI
Description
Fusion Quattro Extraction Balloon FDA UDI

Identifiers

Catalog Number
FS-QEB-B FDA UDI
Primary DI / UDI-DI
00827002482265 EUDAMEDFDA UDI
Basic UDI-DI
0827002WCM00000000047N2 EUDAMED
510(k) Number
K063677 FDA UDI
K200247 FDA UDI
FDA Product Code
GCA FDA UDI
EMDN Code
G03050101 DIGESTIVE ENDOSCOPY, RETRIEVAL BALLOON DEVICES EUDAMED
GMDN Term
ERCP catheter, balloon, non-electrical, stone-retrieval FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
876.5010 FDA UDI
Market of Registration
Germany 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

Yes

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

Fusion Quattro Extraction Balloon by Wilson-Cook Medical, Inc. — 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

EUDAMED SRN
US-MF-000002658
Authorised Representative
COOK MEDICAL EUROPE LIMITED IE-AR-000000907

Sources (2)

  • EUDAMED 26b0586d-01c8-41ba-9e5d-7d92fd07297a 61 fields · synced Jun 18, 2026
  • FDA UDI 19624ee5-eb5d-4431-a3e7-5b38a77bd22d 37 fields · synced May 30, 2026