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Estremo

FDA UDI

Class II (US FDA UDI)

by Citieffe

Identity

Trade Name
ESTREMO FDA UDI
Generic Name
Orthopaedic bone wire FDA UDI
Model / Reference
Kirschner wire, trocar tip ø3x350mm FDA UDI

Identifiers

Catalog Number
643130350 FDA UDI
Primary DI / UDI-DI
08052990976188 FDA UDI
510(k) Number
K181540 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Orthopaedic bone wire FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic bone wire

Estremo by Citieffe — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone wire.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Citieffe

Sources (1)

  • FDA UDI f9d49e44-05b0-4c8b-89a2-3a3ee8069821 36 fields · synced May 30, 2026