St.a.r. 90 F4

FDA UDI

Class II (US FDA UDI)

by Citieffe

Identity

Trade Name: ST.A.R. 90 F4 FDA UDI
Generic Name: Medical ruler, single-use FDA UDI
Model / Reference: Elbow fixator R.O.M. limiter FDA UDI

Identifiers

Catalog Number: F4-2749 FDA UDI
Primary DI / UDI-DI: 08051739535334 FDA UDI
510(k) Number: K113384 FDA UDI
FDA Product Code: KTT FDA UDI
JDW FDA UDI
GMDN Term: Medical ruler, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
888.3040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Medical ruler, single-use

St.a.r. 90 F4 by Citieffe — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K113384 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Citieffe

Sources (1)

FDA UDI 73eb691a-0aa4-4916-94ca-243b839a79cb 36 fields · synced May 30, 2026