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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
External orthopaedic fixation system reprocessed component FDA UDI
Device Name
4922-8-350 11MM MRI CARBON CONNECTING R FDA UDI
Model / Reference
49228350RH FDA UDI
Description
4922-8-350 11MM MRI CARBON CONNECTING R FDA UDI

Identifiers

Catalog Number
49228350RH FDA UDI
Primary DI / UDI-DI
10888277680753 FDA UDI
FDA Product Code
JEC FDA UDI
GMDN Term
External orthopaedic fixation system reprocessed component FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

No

FDA UDI

Manufacturing Date

No

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

Category: External orthopaedic fixation system reprocessed component

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

Similar devices

Also classified as External orthopaedic fixation system reprocessed component.

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 8c61c47c-83a1-4223-85a8-a8ad8798241d 35 fields · synced Jun 7, 2026