Eq-V

FDA UDI

Class I (US FDA UDI)

by Meta Systems Co., Ltd.

Identity

Trade Name: EQ-V FDA UDI
Generic Name: Endodontic obturation system FDA UDI
Device Name: Pack tip (40/03, 50/04) FDA UDI
Model / Reference: EQV-P33 FDA UDI
Description: Pack tip (40/03, 50/04) FDA UDI

Identifiers

Primary DI / UDI-DI: 08809455600771 FDA UDI
FDA Product Code: EKR FDA UDI
GMDN Term: Endodontic obturation system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Endodontic obturation system

Eq-V by Meta Systems Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic obturation system.

EndoPilot D-Pack — Schlumbohm GmbH & Co. KG · Class I
EVOFILL DUO — DiaDent Group International · Class I
Needle — B&L Biotech Co., Ltd. · Class I
Needle — B&L Biotech Co., Ltd. · Class I
DUO-GUN — DiaDent Group International · Class I
EVOFILL DUO — DiaDent Group International · Class I
EVOFILL DUO — DiaDent Group International · Class I
DUO-PEN — DiaDent Group International · 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: Meta Systems Co., Ltd.

Sources (1)

FDA UDI 1b7e2765-1486-454a-b183-a3a1b41c3e5c 33 fields · synced May 30, 2026