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CrossFT

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref CFK-DBP4755

by Conmed Corporation

Identity

Trade Name
CrossFT EUDAMEDFDA UDI
Generic Name
Bone-coring punch, single-use FDA UDI
Device Name
Orthopedic, Non-Active, Instrument, Broaching Punch, Disposable, CrossFT EUDAMED
CROSSFT KNOTLESS 4.75/5.5 BROACHING PUNCH, DISPOSABLE FDA UDI
Model / Reference
CFK-DBP4755 EUDAMEDFDA UDI
Description
CROSSFT KNOTLESS 4.75/5.5 BROACHING PUNCH, DISPOSABLE FDA UDI

Identifiers

Catalog Number
CFK-DBP4755 FDA UDI
Primary DI / UDI-DI
10845854045107 EUDAMEDFDA UDI
Basic UDI-DI
B-10845854045107 EUDAMED
FDA Product Code
HWX FDA UDI
EMDN Code
P091399 ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER EUDAMED
GMDN Term
Bone-coring punch, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Belgium 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Joint prosthesis implantation kit, single-use

CrossFT by Conmed Corporation — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Joint prosthesis implantation kit, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation
EUDAMED SRN
US-MF-000012663
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED cd0d7e4d-4354-43d0-82cc-e22c8a517246 61 fields · synced May 30, 2026
  • FDA UDI cff7d747-8335-4e10-898f-961dd3096538 36 fields · synced May 30, 2026