Conduct

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name: CONDUCT FDA UDI
Generic Name: Composite bone graft FDA UDI
Device Name: CONDUCT Matrix Sponge, 2x5x0.5cm, 10cc (2/box) FDA UDI
Model / Reference: 844.210S FDA UDI
Description: CONDUCT Matrix Sponge, 2x5x0.5cm, 10cc (2/box) FDA UDI

Identifiers

Primary DI / UDI-DI: 00889095333954 FDA UDI
FDA Product Code: MQV FDA UDI
GMDN Term: Composite bone graft FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3045 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Width — 2 Centimeter FDA UDI
Height — 0.5 Centimeter FDA UDI
Total Volume — 10 Milliliter FDA UDI
Length — 5 Centimeter FDA UDI

Category: Composite bone graft

Conduct by Globus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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VENADO Carbonate Apatite Strip — COLLAGEN MATRIX, INC. · Class II
PlatFORM CM Strip — COLLAGEN MATRIX, INC. · Class II
VENADO Carbonate Apatite Putty — COLLAGEN MATRIX, INC. · Class II
VENADO Carbonate Apatite Block — COLLAGEN MATRIX, INC. · Class II

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 II	Pending data

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Manufacturer

Manufacturer: Globus Medical, Inc.

Sources (1)

FDA UDI d2e89b6e-1fc8-46dc-bb58-05a166e67f48 35 fields · synced May 30, 2026