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Arthrex®

FDA UDI

Class II (US FDA UDI)

by Arthrex, Inc.

Identity

Trade Name
Arthrex® FDA UDI
Generic Name
Orthopaedic bone pin, bioabsorbable FDA UDI
Device Name
TRIM-IT DRILL PIN, 1.5MM X 100MM FDA UDI
Model / Reference
AR-4151DS FDA UDI
Description
TRIM-IT DRILL PIN, 1.5MM X 100MM FDA UDI

Identifiers

Catalog Number
AR-4151DS FDA UDI
Primary DI / UDI-DI
00888867032781 FDA UDI
FDA Product Code
HTY FDA UDI
GMDN Term
Orthopaedic bone pin, bioabsorbable 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

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

Yes

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
MRI Safety
MR Safe FDA UDI

Category: Orthopaedic bone pin, bioabsorbable

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

Similar devices

Also classified as Orthopaedic bone pin, bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arthrex, Inc.

Sources (1)

  • FDA UDI df145b89-88ad-4ed3-9e12-05796a97e477 35 fields · synced May 30, 2026