Hollow Drill

FDA UDI

Class I (US FDA UDI)

by Adria Srl

Identity

Trade Name: Hollow Drill FDA UDI
Generic Name: Cannulated surgical drill bit, reusable FDA UDI
Device Name: DRILL FDA UDI
Model / Reference: 495930810 FDA UDI
Description: DRILL FDA UDI

Identifiers

Primary DI / UDI-DI: 08053175004238 FDA UDI
FDA Product Code: HTW FDA UDI
GMDN Term: Cannulated surgical drill bit, reusable 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Cannulated surgical drill bit, reusable

Hollow Drill by Adria Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Cannulated surgical drill bit, reusable.

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EBA2 — Citieffe · Class II
Summa Orthopaedics System Surgical Instrument — Jeil Medical Corporation · Class I
DynaNail — Medshape, Inc. · Class I
BIXCUT — Stryker Corp. · Class I
FREE GLIDING SCFE SCREW SYSTEM — Orthopediatrics Canada ULC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Adria Srl

Sources (1)

FDA UDI 68051118-1c28-41f1-aa49-4e8b71a97929 33 fields · synced May 30, 2026