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Medlineunite

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINEUNITE FDA UDI
Generic Name
Bone graft harvesting filter FDA UDI
Device Name
REAMER, AO/QC, MTP FUSION, MET, 22MM FDA UDI
Model / Reference
MPN20122 FDA UDI
Description
REAMER, AO/QC, MTP FUSION, MET, 22MM FDA UDI

Identifiers

Catalog Number
MPN20122 FDA UDI
Primary DI / UDI-DI
10888277363564 FDA UDI
FDA Product Code
HTO FDA UDI
GMDN Term
Bone graft harvesting filter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone graft harvesting filter

Medlineunite by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone graft harvesting filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI a64bd8c5-17f1-4ad7-b8c4-2c6a594eb3c7 35 fields · synced May 30, 2026