Matira Anterior Cervical System

FDA UDI

Class I (US FDA UDI)

by Kalitec Direct LLC

Identity

Trade Name: MATIRA ANTERIOR CERVICAL SYSTEM FDA UDI
Generic Name: Orthopaedic bone calliper FDA UDI
Device Name: PLATE CALIPER FDA UDI
Model / Reference: 07-K01-3020 FDA UDI
Description: PLATE CALIPER FDA UDI

Identifiers

Catalog Number: 07-K01-3020 FDA UDI
Primary DI / UDI-DI: B07307K0130201 FDA UDI
FDA Product Code: KTZ FDA UDI
GMDN Term: Orthopaedic bone calliper FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4150 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

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: Orthopaedic bone calliper

Matira Anterior Cervical System by Kalitec Direct LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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VerteFIT — Ldr Spine USA · Class I
Perfix™ MIS — CG MedTech Co., Ltd. · 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: Kalitec Direct LLC

Sources (1)

FDA UDI 52af49bf-8c3c-4b3f-ab8e-a3375ae0f930 34 fields · synced Jun 6, 2026