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2.7mm Stepped Drill

FDA UDI

Class I (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
2.7MM STEPPED DRILL FDA UDI
Generic Name
Biopsy drill bit FDA UDI
Model / Reference
24440 FDA UDI

Identifiers

Catalog Number
24440 FDA UDI
Primary DI / UDI-DI
00888480234173 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Biopsy drill bit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

No

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

Category: Biopsy drill bit

2.7mm Stepped Drill by Biomet Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biopsy drill bit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eaadf7db-50fd-4ba2-9d12-c333e355507b 35 fields · synced Jun 1, 2026