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CrossFT

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CrossFT FDA UDI
Generic Name
Orthopaedic broach FDA UDI
Device Name
CrossFT Knotless 4.75 Broaching Punch FDA UDI
Model / Reference
CFK-BP475 FDA UDI
Description
CrossFT Knotless 4.75 Broaching Punch FDA UDI

Identifiers

Catalog Number
CFK-BP475 FDA UDI
Primary DI / UDI-DI
10845854044858 FDA UDI
FDA Product Code
HWX FDA UDI
GMDN Term
Orthopaedic broach FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic broach

CrossFT by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic broach.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 75a5ba98-f5e5-4531-9907-e8879422cd88 36 fields · synced May 30, 2026