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1.5S-Mini Screw

FDA UDI

Class II (US FDA UDI)

by Double Medical Technology Inc.

Identity

Trade Name
1.5S-Mini Screw FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Model / Reference
030070019 FDA UDI

Identifiers

Catalog Number
030070019 FDA UDI
Primary DI / UDI-DI
06942782410230 FDA UDI
510(k) Number
K130108 FDA UDI
FDA Product Code
HRS FDA UDI
HWC FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) 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

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 — 19.0 Millimeter FDA UDI

Category: Orthopaedic bone screw (non-sliding)

1.5S-Mini Screw by Double Medical Technology Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4c9a30ad-02c1-412d-a1d5-5b565751dd4b 36 fields · synced May 31, 2026