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EASE Drilling System

FDA UDI

Class I (US FDA UDI)

by Biomet 3i, Llc

Identity

Trade Name
EASE Drilling System FDA UDI
Generic Name
Fluted surgical drill bit, reusable FDA UDI
Device Name
DRILL KIT TAPERED 4MM X 11.5MM FDA UDI
Model / Reference
DKT411 FDA UDI
Description
DRILL KIT TAPERED 4MM X 11.5MM FDA UDI

Identifiers

Primary DI / UDI-DI
00844868033868 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Fluted surgical drill bit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 11.5 Millimeter FDA UDI

Category: Fluted surgical drill bit, reusable

EASE Drilling System by Biomet 3i, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet 3i, Llc

Sources (1)

  • FDA UDI 903ee0d7-0ffc-44df-a889-8f24380e7dd4 35 fields · synced Jun 8, 2026