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Vilex Cannulated Drill

FDA UDI

Class I (US FDA UDI)

by Vilex In Tennessee, Inc.

Identity

Trade Name
Vilex Cannulated Drill FDA UDI
Generic Name
Fluted surgical drill bit, single-use, non-sterile FDA UDI
Device Name
Drill, Jones Fracture 3.3x175mm FDA UDI
Model / Reference
JF-DRILL-45 FDA UDI
Description
Drill, Jones Fracture 3.3x175mm FDA UDI

Identifiers

Primary DI / UDI-DI
00841731123091 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Fluted surgical drill bit, single-use, non-sterile 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

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

Yes

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: Fluted surgical drill bit, single-use, non-sterile

Vilex Cannulated Drill by Vilex In Tennessee, Inc. — Class I — 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
Vilex In Tennessee, Inc.

Sources (1)

  • FDA UDI baf2936d-2b5b-4e7b-ba1a-fda68cc98a78 33 fields · synced Jun 1, 2026