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Medline Unite

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE UNITE FDA UDI
Generic Name
Surgical drill guide, reusable FDA UDI
Device Name
DBD-DRILL BIT, SOLID CORE, GENERIC, 3.5M FDA UDI
Model / Reference
MPN10035-1 FDA UDI
Description
DBD-DRILL BIT, SOLID CORE, GENERIC, 3.5M FDA UDI

Identifiers

Catalog Number
MPN10035-1 FDA UDI
Primary DI / UDI-DI
10888277694668 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Surgical drill guide, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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: Surgical drill guide, reusable

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

Similar devices

Also classified as Surgical drill guide, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d7725a08-92a2-49a1-b876-3e88d9ceb277 35 fields · synced Jun 8, 2026