← Back to catalogue

Cortical Screw

FDA UDI

Class II (US FDA UDI)

by I.T.S. GmbH

Identity

Trade Name
Cortical Screw FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
Cortical Screw, D=2.7mm, L=15mm FDA UDI
Model / Reference
32271-15 FDA UDI
Description
Cortical Screw, D=2.7mm, L=15mm FDA UDI

Identifiers

Catalog Number
32271-15 FDA UDI
Primary DI / UDI-DI
09120069816006 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) 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: Orthopaedic bone screw (non-sliding)

Cortical Screw by I.T.S. GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
I.T.S. GmbH

Sources (1)

  • FDA UDI 77b1c41e-731f-4c1b-aa8f-f06f0fcb5ca4 34 fields · synced Jun 8, 2026