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Cryoprobe D2.4 mm/13G, 124 mm, Trocar, Spheric

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref FAP7600000

by IceCure Medical Ltd.

Identity

Trade Name
Cryoprobe D2.4 mm/13G, 124 mm, Trocar, Spheric EUDAMED
Cryoprobe D2.4 mm/13G, 124 mm, Trocar, Spheric. FDA UDI
Generic Name
Hand-held cryosurgical system handpiece tip FDA UDI
Device Name
Cryoprobe D2.4 mm/13G, 124 mm, Trocar, Spheric EUDAMED
Cryoprobe-Use only with IceCure Cryogenic Device FDA UDI
Model / Reference
FAP7600000 EUDAMEDFDA UDI
Description
Cryoprobe-Use only with IceCure Cryogenic Device FDA UDI

Identifiers

Catalog Number
FAP7600000 FDA UDI
Primary DI / UDI-DI
07290015487047 EUDAMEDFDA UDI
Basic UDI-DI
B-07290015487047 EUDAMED
510(k) Number
K183213 FDA UDI
FDA Product Code
GEH FDA UDI
EMDN Code
Z120102 CRYOSURGERY EQUIPMENT EUDAMED
GMDN Term
Hand-held cryosurgical system handpiece tip FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
878.4350 FDA UDI
Market of Registration
Italy 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Shaft Length — 124 Millimeter FDA UDI
Needle Gauge — 13 Gauge FDA UDI

Cryoprobe D2.4 mm/13G, 124 mm, Trocar, Spheric by Icecure Medical Ltd. — 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
IL-MF-000026406
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (2)

  • EUDAMED 9d1a9eb8-7bb6-41d7-bd27-9f6a94b034cb 61 fields · synced Oct 5, 2026
  • FDA UDI 5c687da0-a8a6-4cd8-82af-257352950d9a 38 fields · synced May 30, 2026