Microfuse

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name: MICROFUSE FDA UDI
Generic Name: Synthetic bone graft FDA UDI
Device Name: MicroFuse LT Slotted Block, w/BaSO4/CaSO4, 7deg, 14mm x 12mm x 8mm FDA UDI
Model / Reference: 838.014S FDA UDI
Description: MicroFuse LT Slotted Block, w/BaSO4/CaSO4, 7deg, 14mm x 12mm x 8mm FDA UDI

Identifiers

Primary DI / UDI-DI: 00849044043907 FDA UDI
FDA Product Code: MQV FDA UDI
GMDN Term: Synthetic 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 — 14 Millimeter FDA UDI
Height — 8 Millimeter FDA UDI
Length — 12 Millimeter FDA UDI

Category: Synthetic bone graft

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

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Bicera® Resorbable Bone Substitute — WILTROM 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 9b35db9f-ebfd-402d-ba71-a961cb22ec33 35 fields · synced May 30, 2026