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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
Surgical drill chuck FDA UDI
Model / Reference
Chuck for bone screws ø5mm FDA UDI

Identifiers

Catalog Number
SF1080 FDA UDI
Primary DI / UDI-DI
08032909629978 FDA UDI
510(k) Number
K113384 FDA UDI
FDA Product Code
JDW FDA UDI
KTT FDA UDI
GMDN Term
Surgical drill chuck FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.3030 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

No

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: Surgical drill chuck

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

Similar devices

Also classified as Surgical drill chuck.

Cleared under the same submission

K113384 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Citieffe

Sources (1)

  • FDA UDI f7d0a998-07a0-4e60-a5c8-39039afa5a92 36 fields · synced May 30, 2026