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Cannulated Square Driver, 1.7mm

FDA UDI

Class II (US FDA UDI)

by Avanti Orthopaedics Llc

Identity

Trade Name
Cannulated Square Driver, 1.7mm FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Cannulated Square Driver, 1.7mm FDA UDI
Model / Reference
CD17 FDA UDI
Description
Cannulated Square Driver, 1.7mm FDA UDI

Identifiers

Primary DI / UDI-DI
00810054090977 FDA UDI
510(k) Number
K191118 FDA UDI
FDA Product Code
HRS FDA UDI
HWC FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, reusable

Cannulated Square Driver, 1.7mm by Avanti Orthopaedics Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e6bf48f-7a77-4c38-812e-c95292d07acf 35 fields · synced Jun 8, 2026