← Back to catalogue

Quick Connect Screwdriver, Cannulated Silicone Handle

FDA UDI

Class I (US FDA UDI)

by Advanced Orthopaedic Solutions, Inc.

Identity

Trade Name
QUICK CONNECT SCREWDRIVER, CANNULATED SILICONE HANDLE FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Model / Reference
0453 FDA UDI

Identifiers

Primary DI / UDI-DI
00848665001938 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical screwdriver, 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, reusable

Quick Connect Screwdriver, Cannulated Silicone Handle by Advanced Orthopaedic Solutions, Inc. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4ec62e14-02f5-4699-b9ac-210466e134cf 32 fields · synced May 30, 2026