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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Orthopaedic bone screw starter/notcher FDA UDI
Device Name
DRILL BIT, SOLID CORE, AO/QC, 2.0MM FDA UDI
Model / Reference
MPN10020 FDA UDI
Description
DRILL BIT, SOLID CORE, AO/QC, 2.0MM FDA UDI

Identifiers

Catalog Number
MPN10020 FDA UDI
Primary DI / UDI-DI
10888277363380 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic bone screw starter/notcher FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

No

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
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2 Millimeter FDA UDI

Category: Orthopaedic bone screw starter/notcher

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw starter/notcher.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f4d1a05-1e83-4168-afee-e1d79edfd64c 37 fields · synced May 30, 2026