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4.0mm Cannulated Screw

FDA UDI

Class II (US FDA UDI)

by Double Medical Technology Inc.

Identity

Trade Name
4.0mm Cannulated Screw FDA UDI
Generic Name
Pin-sleeve orthopaedic bone screw FDA UDI
Model / Reference
060020040 FDA UDI

Identifiers

Catalog Number
060020040 FDA UDI
Primary DI / UDI-DI
06942782409272 FDA UDI
510(k) Number
K130108 FDA UDI
FDA Product Code
HWC FDA UDI
HRS FDA UDI
GMDN Term
Pin-sleeve orthopaedic bone screw 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 40.0 Millimeter FDA UDI

Category: Pin-sleeve orthopaedic bone screw

4.0mm Cannulated Screw by Double Medical Technology Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pin-sleeve orthopaedic bone screw.

Cleared under the same submission

K130108 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Double Medical Technology Inc.

Sources (1)

  • FDA UDI 26371953-d7d3-4cd5-a2b7-50a836783cd8 36 fields · synced May 30, 2026