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2.5mm Drill

FDA UDI

Class II (US FDA UDI)

by Miami Device Solutions

Identity

Trade Name
2.5mm Drill FDA UDI
Generic Name
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile FDA UDI
Device Name
2.5mm Drill FDA UDI
Model / Reference
MDS111125150 FDA UDI
Description
2.5mm Drill FDA UDI

Identifiers

Catalog Number
MDS111125150 FDA UDI
Primary DI / UDI-DI
10812269020487 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

Yes

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: Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterileFluted surgical drill bit, single-use, non-sterile

2.5mm Drill by Miami Device Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, single-use, 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 9c9dca05-7863-4428-9441-2ca7cf377644 35 fields · synced Jun 8, 2026