← Back to catalogue

Echotip Ultra

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref ECHO-3-22

by Wilson-Cook Medical, Inc.

Identity

Trade Name
EchoTip FDA UDI
Generic Name
Ultrasound aspiration biopsy procedure kit FDA UDI
Device Name
ECHOTIP ULTRA EUDAMEDFDA UDI
Model / Reference
ECHO-3-22 EUDAMED
G31521 FDA UDI
Description
Echotip Ultra FDA UDI

Identifiers

Catalog Number
ECHO-3-22 FDA UDI
Primary DI / UDI-DI
00827002315211 EUDAMEDFDA UDI
Basic UDI-DI
B-00827002315211 EUDAMED
FDA Product Code
FCG FDA UDI
EMDN Code
A01020102 ASPIRATION FINE NEEDLES AND KITS EUDAMED
GMDN Term
Ultrasound aspiration biopsy procedure kit FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.1075 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

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

Echotip Ultra by Wilson-Cook Medical, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

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 818a2414-df6d-46d5-92ce-a83e46fade0a 61 fields · synced May 30, 2026
  • FDA UDI 9a530f7b-7a28-4072-8862-035979f5f4ff 36 fields · synced May 30, 2026