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Individual Package Drill Bit, D:3.5mm

FDA UDI

Class I (US FDA UDI)

by Flower Orthopedics Corporation

Identity

Trade Name
Individual Package Drill Bit, D:3.5mm FDA UDI
Generic Name
Screwing power tool attachment FDA UDI
Device Name
surgical instrument or accessory for orthopedic bone fixation FDA UDI
Model / Reference
FDB 035 FDA UDI
Description
surgical instrument or accessory for orthopedic bone fixation FDA UDI

Identifiers

Primary DI / UDI-DI
00840118111867 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Screwing power tool attachment 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

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

Category: Screwing power tool attachment

Individual Package Drill Bit, D:3.5mm by Flower Orthopedics Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Screwing power tool attachment.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e2b9406b-358b-49bd-962c-5b5bb4c210ae 33 fields · synced Jun 8, 2026