SCANLAN® Instrumentation

FDA UDI

Class I (US FDA UDI)

by Scanlan International Inc

Identity

Trade Name: SCANLAN® Instrumentation FDA UDI
Generic Name: Wire-extracting pliers FDA UDI
Device Name: Kerrison Style Wire Cutter FDA UDI
Model / Reference: Q39035-09 FDA UDI
Description: Kerrison Style Wire Cutter FDA UDI

Identifiers

Catalog Number: Q39035-09 FDA UDI
Primary DI / UDI-DI: 00846159033656 FDA UDI
FDA Product Code: HXZ FDA UDI
GMDN Term: Wire-extracting pliers 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

FDA UDI

Single Use

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

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Wire-extracting pliers

SCANLAN® Instrumentation by Scanlan International Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire-extracting pliers.

gSource — GSOURCE, LLC. · Class I
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Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
WIRE EXTRACTION PLIERS — SONTEC INSTRUMENTS, INC. · Class I
PIN PULLER — SONTEC INSTRUMENTS, INC. · Class I
gSource — GSOURCE, LLC. · Class I
AESCULAP — AESCULAP, INC. · Class I
AESCULAP — AESCULAP, INC. · Class I

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: Scanlan International Inc

Sources (1)

FDA UDI 6e827611-87f1-41ab-91d0-02237cd6d679 35 fields · synced May 30, 2026