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Dyonics

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
DYONICS FDA UDI
Generic Name
Fluted surgical drill bit, reusable FDA UDI
Device Name
DYONICS SST STD TWIST DRILL 2.0MM X 127M FDA UDI
Model / Reference
72204445 FDA UDI
Description
DYONICS SST STD TWIST DRILL 2.0MM X 127M FDA UDI

Identifiers

Catalog Number
72204445 FDA UDI
Primary DI / UDI-DI
00885554036190 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Fluted surgical drill bit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

No

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: Fluted surgical drill bit, reusable

Dyonics by Smith & Nephew, Inc. — 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

Sources (1)

  • FDA UDI c5fbd5c5-5b21-480a-a6eb-9daef70a05fa 35 fields · synced Jun 8, 2026