Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name: Medline FDA UDI
Generic Name: Bone-resection orthopaedic reamer, reprocessed FDA UDI
Device Name: 5091-143 MICRO BUR,SWANSON REAMER,MD, FDA UDI
Model / Reference: 5091143R FDA UDI
Description: 5091-143 MICRO BUR,SWANSON REAMER,MD, FDA UDI

Identifiers

Catalog Number: 5091143R FDA UDI
Primary DI / UDI-DI: 10888277385566 FDA UDI
FDA Product Code: GFF FDA UDI
GMDN Term: Bone-resection orthopaedic reamer, reprocessed FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Bone-resection orthopaedic reamer, reprocessed

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

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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 I	Pending data

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Manufacturer

Manufacturer: Medline Industries, Inc.

Sources (1)

FDA UDI 4637fde3-f5d5-4168-8958-0212378a2ac6 35 fields · synced May 29, 2026