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AlloFuse® Plus

FDA UDI

Class II (US FDA UDI)

by Allosource

Identity

Trade Name
AlloFuse® Plus FDA UDI
Generic Name
Bone matrix implant, human-derived FDA UDI
Device Name
AlloFuse® Plus DBM Paste, 1 cc FDA UDI
Model / Reference
90238001 FDA UDI
Description
AlloFuse® Plus DBM Paste, 1 cc FDA UDI

Identifiers

Catalog Number
90238001 FDA UDI
Primary DI / UDI-DI
M536902380011 FDA UDI
FDA Product Code
MQV FDA UDI
MBP FDA UDI
GMDN Term
Bone matrix implant, human-derived 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

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

Yes

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone matrix implant, human-derived

AlloFuse® Plus by Allosource — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone matrix implant, human-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allosource

Sources (1)

  • FDA UDI 2d6ec599-95e1-44e4-8181-89231f4b0c16 36 fields · synced May 30, 2026