Cannulated Drill Bit, 1.7mm

FDA UDI

Class I (US FDA UDI)

by Flower Orthopedics Corporation

Identity

Trade Name: Cannulated Drill Bit, 1.7mm FDA UDI
Generic Name: Cannulated surgical drill bit, single-use FDA UDI
Device Name: Cannulated surgical drill bit, single-use, sterile FDA UDI
Model / Reference: CDB 217 FDA UDI
Description: Cannulated surgical drill bit, single-use, sterile FDA UDI

Identifiers

Primary DI / UDI-DI: 00840118118385 FDA UDI
FDA Product Code: HTW FDA UDI
GMDN Term: Cannulated surgical drill bit, single-use 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

FDA UDI

Dimensions & Sizes

Size: Length — 110 Millimeter FDA UDI
Outer Diameter — 1.7 Millimeter FDA UDI

Category: Cannulated surgical drill bit, single-use

Cannulated Drill Bit, 1.7mm by Flower Orthopedics Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Flower Orthopedics Corporation

Sources (1)

FDA UDI 0b5bf745-bc27-403d-8677-c4f4cd0e1d5b 35 fields · synced Jun 6, 2026