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Cannulated Hexalobe Screw Driver

FDA UDI

Class II (US FDA UDI)

by Miami Device Solutions

Identity

Trade Name
Cannulated Hexalobe Screw Driver FDA UDI
Generic Name
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile FDA UDI
Device Name
Cannulated Hexalobe Screw Driver, AO, X15 FDA UDI
Model / Reference
MDS110404AO FDA UDI
Description
Cannulated Hexalobe Screw Driver, AO, X15 FDA UDI

Identifiers

Catalog Number
MDS110404AO FDA UDI
Primary DI / UDI-DI
10812269021750 FDA UDI
FDA Product Code
HWC FDA UDI
HRS FDA UDI
GMDN Term
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, reusableInternal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Cannulated Hexalobe Screw Driver by Miami Device Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Miami Device Solutions

Sources (1)

  • FDA UDI 0c2a9943-60b5-4c77-9426-a108c48ce399 35 fields · synced May 31, 2026