Arthrex®

FDA UDI

Class I (US FDA UDI)

by Arthrex, Inc.

Identity

Trade Name: Arthrex® FDA UDI
Generic Name: Surgical tissue compression device FDA UDI
Device Name: Univers VaultLock Graft Compression Tool FDA UDI
Model / Reference: AR-9236GT FDA UDI
Description: Univers VaultLock Graft Compression Tool FDA UDI

Identifiers

Catalog Number: AR-9236GT FDA UDI
Primary DI / UDI-DI: 00888867254732 FDA UDI
FDA Product Code: MDM FDA UDI
GMDN Term: Surgical tissue compression device FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical tissue compression device

Arthrex® by Arthrex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical tissue compression device.

BR Surgical, LLC — BR SURGICAL LLC · Class I
FENTEX — FENTEX medical GmbH · Class I
GUBISCH CARTILAGE CRUSHER — SONTEC INSTRUMENTS, INC. · Class I
V. Mueller — STERIS CORPORATION · Class I
Symmetry Cottle — SYMMETRY SURGICAL INC. · Class I
Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC · Class I
EVONOS — Gyrus Acmi, Inc. · Class I
BOSS Instruments — Boss Instruments, 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

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

Manufacturer

Manufacturer: Arthrex, Inc.

Sources (1)

FDA UDI 3fc50123-a1bf-4369-92c1-f9b3c1e342f8 35 fields · synced May 30, 2026