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MgNum

FDA UDI

Class II (US FDA UDI)

by Paragon 28

Identity

Trade Name
MgNum FDA UDI
Generic Name
Bone graft delivery kit FDA UDI
Device Name
MgNum, Bone Void Filler, Mixing and Delivery System FDA UDI
Model / Reference
P02-BVF-AUX1 FDA UDI
Description
MgNum, Bone Void Filler, Mixing and Delivery System FDA UDI

Identifiers

Catalog Number
P02-BVF-AUX1 FDA UDI
Primary DI / UDI-DI
00889795111005 FDA UDI
FDA Product Code
MQV FDA UDI
GMDN Term
Bone graft delivery kit 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Bone graft delivery kit

MgNum by Paragon 28 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone graft delivery kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 12a60ae9-5aad-42a9-99cf-38cdff22de38 34 fields · synced Jun 1, 2026