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Ilizarov Systems

FDA UDI

Class II (US FDA UDI)

by Medicalplastic Srl

Identity

Trade Name
ILIZAROV SYSTEMS FDA UDI
Generic Name
External orthopaedic fixation system, single-use FDA UDI
Device Name
THREADED ROD SLOTTED 60MM LENGTH FDA UDI
Model / Reference
102401 FDA UDI
Description
THREADED ROD SLOTTED 60MM LENGTH FDA UDI

Identifiers

Catalog Number
102401 FDA UDI
Primary DI / UDI-DI
28033201841895 FDA UDI
510(k) Number
K994143 FDA UDI
FDA Product Code
JDW FDA UDI
GMDN Term
External orthopaedic fixation system, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: External orthopaedic fixation system, single-use

Ilizarov Systems by Medicalplastic Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External orthopaedic fixation system, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medicalplastic Srl

Sources (1)

  • FDA UDI 5968eac7-d38e-440a-9cdb-23799dc38a71 35 fields · synced Jun 1, 2026