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Orthopaedic Surgical Instruments

FDA UDI

Class I (US FDA UDI)

by Citieffe

Identity

Trade Name
Orthopaedic Surgical Instruments FDA UDI
Generic Name
Orthopaedic bone-fragment manipulator, reusable FDA UDI
Device Name
Talo-calcaneal compression device FDA UDI
Model / Reference
Compaction device FDA UDI
Description
Talo-calcaneal compression device FDA UDI

Identifiers

Catalog Number
DT030952 FDA UDI
Primary DI / UDI-DI
08059386743478 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic bone-fragment manipulator, reusable 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic bone-fragment manipulator, reusable

Orthopaedic Surgical Instruments by Citieffe — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone-fragment manipulator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Citieffe

Sources (1)

  • FDA UDI 1ff49713-ef78-4774-b52c-62bf3e6d47f2 36 fields · synced Jun 8, 2026